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ACRP 2014 Global Conference & Exhibition
 
ACRP 2015 Global Conference & Exhibition
 
ACRP 2016 Meeting & Expo
 
Site Strategy Forum 2015
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"An Aerial View of Forces Reshaping the Global Clinical Research Enterprise" Keynote Presentation with Ken Getz
 
2014 Annual Update of U.S. Healthcare Regulations Impact on Clinical Research Industry
 
2015 Update: U.S. Healthcare Changes and How They Affect the Clinical Research Industry
 
2015 Update: U.S. Healthcare Changes and How They Affect the Clinical Research Industry (REPEAT)
 
2016 Update: U.S. Healthcare Changes and How They Affect the Clinical Research Industry
 
5 Communication Tactics: Maximizing Recruitment, Retention
 
7 Year Itch; Hidden Cost of Conducting Clinical Trials
 
FREE SESSION - An FDA Inspection of a Clinical Research Site: Part 1
 
A Bespoke Model for Recruiting and Retaining Hispanic Patients
 
A Creative Solution to Staffing in a Competitive Hiring Environment
 
A Demographic Analysis of the U.S. IRB Registration Database
 
A GCP Update from the FDA's Perspective
 
A Lesson from Broadway: Setting the Stage for Successful Research Projects through Protocol Feasibility
 
A New Data Collection Model to Streamline Data Flow, Traceability and Transparency
 
A New Philosophy in Research -Transformation of the Scientist, Institution, Research, Health Practice, Industry and Community to Improve Health Care
 
A Revitalized and Streamlined Clinical Advancement Program That Recognizes, Rewards and Retains Expert Clinical Research Nurses At Academic Medical Centers
 
A Road Map to Quality Systems/SOPs at the Site
 
A Systems Approach to Suicide in the Military - NOT RECORDED
 
A Trainer's Arsenal of Assessment Tools for Different Venues
 
A Turbo Tax ?Approach: How One Academic Medical Center Converted to a Streamlined, Paperless Institutional Review Board
 
ABCs of Posting Study Results - Making It Easy
 
Academia, Investigator-Initiated Research and a Unique Resource to Support Both
 
Acceptability of Foreign Clinical Data from Non-IND Studies
 
Accounts Receivable for Research Sites: Closing the Gap between Service and Payment
 
Accurate Budgeting for Patient Recruitment
 
ACRP Business Meeting
 
ACRP Business Meeting
 
Adapt or Perish? The Evolving Clinical Research Professional
 
Adaptive Designs and their Challenges for Clinical Sites
 
Addressing "Drug Developability" in Early Clinical Development: Application of New Technologies and Approaches
 
Addressing Critical Needs: Program for Advancing Coordinator Training, Leadership and Certification in an Academic Medical Center
 
Addressing Linguistic & Cultural Barriers in Global Trials - NOT RECORDED
 
Addressing the Clinical Research Associate Shortage: A Proposal to Industry
 
Addressing the Shortage: How to Develop Good CRAs
 
Adjudication of Serious Adverse Events by an External Committee in a Large Safety Trial
 
Advanced Business Concepts in Research for Physicians
 
Advanced Monitoring Visit Documentation: Global Regulatory Authority Inspections and Sponsors
 
Advances in Clinical Research on Sport-Related Concussion
 
Adverse Event and Technical Observations in Medical Device Trials – What's the Difference?
 
Adverse Event Reporting - NOT RECORDED
 
Adverse Event Reporting in Medical Device Trials - FDA Panel Discussion
 
Advertising that Works!
 
Advice from a Hired Gun in Clinical Trial Litigation
 
Aligned and Harmonized Core Competencies for the Clinical Research Enterprise - As Defined by the Joint Task Force for Clinical Trial Competency
 
Aligning Centralized and Site-Based Monitoring: Optimizing Quality Outcomes
 
Aligning Expectations: Collaboration in the Multi-Specialty Site
 
Aligning the Documents ? One Step to Reducing Chaos
 
All-Inclusive Budgeting for Research Sites
 
Alternative Study Designs for Medical Devices: Standardized Objective Performance Criteria (OPCs) and Controlled Data Sets
 
Alternatives for Classroom Training
 
AMC Forum Session: Perspectives on Investigator Initiated Trials
 
An Academic Medical Center Based Coordination Center for Multi-center Trials (AMC-CC): Balancing Resources, Funding and Demands
 
An Academic Question: Who Does Clinical Research Best?
 
An Afternoon with Eva Mozes-Kor - Special Event
 
An Analysis of Site Monitoring Reports: It's a Lot More than the Follow-up Letter!
 
An Approach to Quality Management in an Academic Setting
 
An Educator Toolbox: Tools for Different Training Venues
 
An Effective Corrective and Preventive Action Program (CAPA)
 
An FDA Clinical Inspection -- Are You Prepared?
 
An FDA Inspection Preparedness Framework: A Large, Multi-National Clinical Trial
 
An Idea Whose Time Has Come: Next Steps in the Professionalization of Clinical Research
 
An IRB's Experience with Investigator Non-Compliance - A Real-World Case History
 
An Update on Advances in Clinical Research on Sport-related Concussion
 
An Update on FDA Good Clinical Practice Activities
 
Analysis of the Microbiome in Health and Disease
 
APPI Presidential Address
 
APPI Presidential Address: Clinical Research in the Era of Reality TV: Are We Dancing with the Stars?
 
Application of Genomics and Proteomics in Pre-Clinical Research
 
Applying a Quality Systems Approach to Clinical Device Research
 
Approach to the Regulation of Subsequent Entry Biologics (SEB) in Canada
 
Are Minorities LIKEing You? Social Media in Minority Recruitment/Retention
 
Are You Ready for a Sponsor BIMO Inspection: Experiences from a Medical Device Sponsor and CRO's Mock FDA Inspection
 
Around the World in 120 Minutes: A Discussion of Global Research
 
As Clear as Mud: Investigator-Initiated Research in Canada
 
Assenting in the Pediatric Oncology Setting
 
Assessing Investigator Oversight
 
Assessing the Impact of Protocol Design Change on Study Conduct Performance
 
Assessing Workplace Competencies of CRAs: A SA Proposal
 
Asynchronous vs. Synchronous Training...How to Choose? - NOT RECORDED
 
At Your Service: Making Patient Relations a Priority at Your Site
 
Audit Aftermath - Does CAPA Help?
 
Autism and Vaccines - Research Misconduct and Fraud Has Real Consequences
 
Avoiding Pitfalls and Failure in Product Development (Plenary Closing Session)
 
Avoiding the Leap from 483 to Warning Letter - Lessons Learned
 
Back to Basics: Lab Training
 
Basic Oncology Concepts for the Research Professional
 
Basic Overview of Medical Devices in a Global Market
 
Beam Me the Data Scotty! Site Monitoring Without the Plane
 
Because It's GCP!
 
Before RBM was in Vogue: How NIH Managed Efficient Monitoring
 
Bench to Bedside: The Role of Translational Research in the Scientific Arena
 
Bench to Patient: The Device Regulatory Process
 
Benchmarks in Clinical Trial Management
 
Benchmarks in Clinical Trial Management - A Follow Up to 2009
 
Best Practices in Conducting IVD Clinical Trials
 
Best Practices in Study Start-Up Activities
 
Best Practices: Tips for Enhancing Your Investigator Skills
 
Biobanking and Future Research: Insights to a More Meaningful and Compliant Consent Process
 
Bioethics and Biomarkers: Protection of Human Subjects in the 'Omics Age'
 
Bioresearch Monitoring in Medical Devices: Practical Considerations when Preparing for and Responding to FDA Inspections
 
Bioresearch Monitoring in Medical Devices: Practical Considerations when Preparing for and Responding to FDA Inspections
 
Biostatistics in Clinical Research
 
Book Review: A Novel Approach to Clinical Research Education - NOT RECORDED
 
Boots on Deck: Project Management in the Trenches
 
Brain Tumors Under Attack: The "Shock and Awe" of Oncolytic Viruses
 
Breaker, Breaker 1-9: Effective Communication Strategies - NOT RECORDED
 
Bridging the Gap: Improving Communications Between Clinical Operations and Data Management
 
Building a Better Budget: How Budget Improves Clinical Trials
 
Building Quality Into Clinical Trials: FDA and Medical Device Perspectives
 
Building Standards for Research Ethics Boards in Canada
 
Busting the Myths of Oncology Research
 
Can Academic Medical Centers Effectively Sponsor Multi-Site Trials?
 
Can We Really Improve Study Management at an Academic Medical Center (AMC)?
 
Can You Hear Me? Communication in Clinical Research
 
Can You Imagine Yourself a Clinical Research Participant?
 
Cannabinoid Clinical Trials: Current Review, Problems, Pitfalls and Solutions
 
CAPA Isn't Just a Compliance Tool: Maximizing Site Performance Applying CAPA Principles
 
Case Studies in Pediatric Research
 
Case Study: eConsents on the iPad
 
Case-control Analysis of Combat-Associated Acute Lung Injury
 
CDER BIMO Compliance and Enforcement - Before, During and After an Inspection
 
CDER BIMO Compliance and Enforcement - What You Need to Know!
 
CDER BIMO Compliance and Enforcement: What You Need to Know
 
CDER BIMO Compliance and Enforcement: What You Need to Know!
 
CDISC and the Critical Path Institute: Collaborative Research and Standards to Innovate Therapy Development
 
CDISC Standards WILL be Required for Device Companies!
 
CDRH BIMO Inspection Program: Site Readiness from IDE through PMA
 
Center for Drug Evaluation and Research (CDER) Bioresearch Monitoring Inspections (BIMO) and Warning Letters
 
Centralized Files at an Investigative Site - NOT RECORDED
 
Challenges of Translation Process in Multinational Research Program Across Africa
 
Challenges to Conducting Clinical Trials in Japan - NOT RECORDED
 
Civil and Criminal Liability from Clinical Trials: What are the Legal Risks?
 
Clean Data and Complex Trials: Can this Marriage be Saved? - NOT RECORDED
 
Clear the Mud: Current and Future of Cannabis Research
 
Clinical & Data Management: Partnering to Ensure Electronic Data Capture (EDC) Success - NOT RECORDED
 
Clinical Data Management System Validation
 
Clinical Data, EHR, Informed Consent and Privacy: What Are the Rules and How to Ensure Compliance?
 
Clinical Design and Statistics in Sponsored Trials
 
Clinical Leadership: Exploring New Strategies for Service and Professionalization
 
Clinical Research and the Bedside Nurse: Making it Better - NOT RECORDED
 
Clinical Research Associate Mentoring Program - NOT RECORDED
 
Clinical Research Billing Compliance and Revenue Cycle Management: Current Trends
 
Clinical Research Billing Compliance: Challenges and Solutions
 
Clinical Research Billing: The Crossroads of Clinical Research Compliance
 
Clinical Research Data Standards - An Idea Whose Time Has Come
 
Clinical Research Degree Programs in the United States: Their Need and Availability
 
Clinical Research Education in Asia - Focus on the Indian Sub Continent
 
Clinical Research Education: Plant the Seed, Watch it Grow!
 
Clinical Research Feud - And the Survey Says!!!
 
Clinical Research in Argentina Today
 
Clinical Research in Canada
 
Clinical Research in China, the EU and the US: A Device Perspective
 
Clinical Research in Dentistry: Advantages and Concerns
 
Clinical Research in Latin America - A Device Perspective
 
Clinical Research Liability Update
 
Clinical Research Management System (CRMS): Improved Efficiency Through Systems Integration - NOT RECORDED
 
Clinical Site Selection: Standardizing the Process
 
Clinical Study Delivery Using Functional Service Providers
 
Clinical Study Risk Management - NOT RECORDED
 
Clinical Trial Agreements for Medical Device Sponsors
 
Clinical Trial Billing: Solutions to a Complex Problem
 
Clinical Trial Data Management Systems - Increased Efficiency or Increased Workload?
 
Clinical Trial Designs in the Era of Personalized Genomics
 
Clinical Trial Disclosure - Are You Compliant?
 
Clinical Trial Disclosure Requirements: A Moving Target
 
Clinical Trial Globalization: An Examination of Factors Driving Clinical Trials to Emerging Markets and the Impact on Patient Recruitment and Site Selection
 
Clinical Trial Globalization: Hype vs. Reality
 
Clinical Trial Registries: Panacea or Pablum?
 
Clinical Trial Registries: Panacea or Pablum?
 
Clinical Trial Start-Up, Contingency & Enrollment Planning
 
Clinical Trial Study Management Plans: The Architecture of a Quality Clinical Trial
 
Clinical Trials Contracting Efficiency: A Means to Save Millions
 
Clinical Trials in Canada: A Regulatory Review
 
Clinical Trials in China
 
Clinical Trials in India: Ethical and Operational Challenges
 
Clinical Trials Opportunities and Challenges - Middle East and North Africa (MENA) Region
 
Clinical Trials Transformation Initiative (CTTI)
 
Clinical Trials Using Decisionally Impaired Subjects: The Markingson Case
 
Clinical Vendor Selection for Emerging Clients
 
Coercion and Clinical Research
 
Collaboration in Medical Device Clinical Trial Innovation and Reform
 
Collaboration in Patient-Centered Medical Device Innovation and Regulation
 
Common Clinical Trial Designs for Medical Devices
 
Communication Strategies for Conflict Resolution in Clinical Research Teams
 
Community Outreach: Feet on the Street
 
Comparative Effectiveness Trials: Challenges & Opportunities
 
Comparing and Contrasting Safety Reporting in Drug and Device Trials
 
Comparing FDA & Health Canada Research Requirements
 
Comparing ICH E6 with ISO 14155 Medical Device GCPs
 
Competence of Research Ethics Committees in Patient Protection
 
Competency-Based Assessment of Clinical Research Education and Training Needs
 
Concentration Effect Relationship and Disease Models - The Mechanistic Framework of Drug Development and Regulation
 
Conduct of Clinical Research: Liability of Sponsors and Sites
 
Conducting Clinical Research in SE Asia
 
Conducting Clinical Trials in China: Status and Trends
 
Conducting Effective CRA Preceptor Visits
 
Conducting First-in-Human Studies - Is Your Site Prepared?
 
Conducting Global Clinical Research in a Virtual World
 
Conducting Successful Clinical Trials in Japan: Collaboration, Culture and Change
 
Conducting Trials Involving Pediatric Populations: Considerations for Clinical Research Professionals
 
Conflict of Interest or Conflict of Care?
 
Conflict Resolution: Helping Teams Manage Through Conflict
 
Connecting to Diversity Populations: When Recruitment Goes Digital
 
Connecting with the Other "Half" in Clinical Research Recruitment - The Forgotten Majority
 
Consenting and Enrolling People with Physical Impairments and Disabilities
 
Considerations for Software Validation
 
Contracting 101: The Dos and Don'ts to Get You Started
 
Cost Effectiveness: Sometimes the Simplest Studies Yield the Biggest Results
 
Could Research Billing be the Faulty O-Ring of Your Organizational Shuttle?
 
Coverage Analysis, Budgeting and Pre-Award Practices Limiting Fiscal Risk in Clinical Research
 
CRA Persona: Dr. Jekyll or Mr. Hyde?
 
CRAs & CRCs: Playing Nice on the Clinical Research Field
 
CRAs as Site Recruitment Managers: Point-Counter Point
 
CRAs in 2010 and 2020: CRA Career Ladder Survey II
 
CRC Forum Session: Ethical Issues for Clinical Research Coordinators
 
Create a Culture of Ethics and Compliance in Clinical Trial Billing and Reimbursement
 
Create an Onboarding Curriculum that Fits Your Budget
 
Creating a Strategic Clinical Study Plan for Medical Devices
 
Creating A Successful Relationship Between Independent CRA and CRO
 
Creating Accountability: A Step-by-Step Approach
 
Creating and Documenting Your Informed Consent Process
 
Creating and Fostering a Culture of Quality and Compliance
 
Creating Effective Pediatric Assent Forms: Overcoming Common Obstacles
 
Creating SOPs for a Clinical Trial Investigative Site - NOT RECORDED
 
Creation and Implementation of a CRC Education and Mentoring Program
 
Creative and Critical Thinking in a Regulated Environment
 
CRO Budgets
 
CTTI - INVITED
 
CTTI Use of Central IRBs for Multicenter Clinical Trials
 
Current Issues in Conducting IVD Clinical Trials
 
Current Practices and Issues Surrounding Clinical Trial Agreements: Is There a Problem?
 
Current Situation and Challenges of Clinical Trials in Japan
 
Current Situation of Clinical Trials in Japan
 
Current Trends in Global Drug Development Involving Japan
 
Current Trends, Best Practices in VA Research Compliance
 
Customer Relationship Management (CRM) & Media Buying 101
 
Customer Relationship Management: Getting The Most Out of Patient Recruitment Referrals
 
Customizing EMR Functionality To Maximize Participation in Clinical Trials
 
Cut the Queries! Collaborating for Increased Efficiency in the Query Process
 
Data Collection: From the Source to Data Analysis and Everything in Between
 
Data Management & Technology Forum Session: Blended Technology Solutions Proven to Minimize "Trial Drift" in Clinical Research
 
Data Management for Non-Data Managers
 
Data Manager and CRA Collaboration in an eClinical Environment - Working Together for Quality Data - NOT RECORDED
 
Data Quality & Integrity: From Monitoring to Approval
 
Data Safety Monitoring Committees—What, Why, When, How
 
Data-Mining in Observational Research: Helping to Answer Clinically Relevant Questions
 
Dealing with Noncompliance and Mitigating the Risk
 
Dealing with Unanticipated Problems Involving Risk in Clinical Research
 
Debate Under Oxford Rules
There will be no slides for this session.
 
Decoding the New Drug Good Clinical Practice Regulations
 
Dedicated Site Selection Teams to Speed Study Start Up
 
Defending Your Informed Consent Process
 
Delegation of Site Duties for CRAs, Sites and Sponsors
 
Demystifying the Drug Development Process at the FDA: What is the Fuss?
 
Deploying the Best Study Feasibility Model to Predict Success Early and Often
 
Design the Future of Our Profession as a Profession
 
Design the Future of Our Profession as a Profession
 
Designing a Device Clinical Trial
 
Develop Master Trainer CRAs for a High Performing Team
 
Developing a Clinical Trials Office Outside the Academic Medical Center
 
Developing a Comprehensive Research Education Program
 
Developing a Mechanism to Determine Protocol Complexity for a Diverse Research Site
 
Developing a Winning Relationship with Your Biostatistician
 
Developing and Sustaining a Team Effort in Clinical Research Settings
 
Developing Evidence-based Research Competencies: Tracking Progress from Novice to Expert
 
Development and Implementation of a Performance Report Card in a Multi-center Research Network
 
Development and Implementation of a Phase I Unit for Rheumatology
 
Development of Distance Learning Technologies for Clinical Research Education
 
Device and Drug Development: Similarities and Differences Explored
 
Device Forum Session: Regulatory and Design Considerations for Clinical Research of Medical Devices
 
Device Post-Approval Studies: FDA Panel Discussion
 
Device Recalls and Safety Alerts During a Clinical Trial
 
Device Recalls and Safety Alerts During a Clinical Trial
 
Device Trials - A Good Business Decision for Academic Medical Centers (AMCs)? - NOT RECORDED
 
Device Trials, Quality Data, and High Enrollment Numbers: How to Get It All
 
Device: Post Approval Studies
 
Distance-Based Education for Foreign Study Coordinators - NOT RECORDED
 
Documentation & Auditing: The Bilingual Consent Aide Process - NOT RECORDED
 
Drug and Device Clinical Research Compared and Contrasted
 
Drug Development - Today and Tomorrow
 
Drugs and Devices - What's the Difference?
 
E&R Forum Session: Ethics without Borders - Facing the Challenges of Globalization in Clinical Research and Subject Protection
 
E-Consents 101 - The Benefits and Potential Obstacles Associated with Electronic Consent for Clinical Trials
 
E-Consents 101: The Why, How, and Watch-Outs of Moving to Electronic Consent for Clinical Trials
 
E-Labeling - Options and Clinical Study Impact
 
E-Labeling: Pros and Cons
 
e-Tools for Improving Monitoring Efficiency On-site and Off
 
Ebola and other Emerging Pathogens - A New Challenge for Research and Healthcare
 
Educate, Inform and Promote: Making Public Relations Successful For Your Site
 
Education, A Tool to Overcome the Shortage in Skillful Clinical Research Staff
 
Effective Communication to Manage Difficult Relationships
 
Effective Development, Management and Utilization of Study Websites
 
Effective Employee Training for a Multi-Generational Workforce
 
Effective Monitoring? May the Source be With You!
 
Effective Pharmacovigilance: A Global Case Study
 
Effective Training of Study Staff for Better Clinical Trials
 
Efficiencies Gained Using a Site/CRO Preferred Partnership Model
 
Electrifying Research: EMR, eCRF and Clinical Research
 
Electronic Health Records - Changing the Face of Research?
 
Electronic Health Records to Optimize Trial Recruitment
 
Electronic Media for Patient Recruitment and Site Branding
 
Electronic Medical Records: What Sites and Sponsors/Monitors Should Understand about Basic Part 11 Implications
 
Electronic Patient Reported Outcome in Clinical Trials: An Overview
 
Eliminating Shadow Charts from Your Study Site
 
Embedded Partnership Site Model for Private Practices
 
Emergency Equipment and Training in Clinical Trials
 
Emerging Biotherapeutics: The Essential Role of Adaptive Clinical Research
 
Emerging Quality Trends from Regulatory Authorities: Qualifications And Training of Staff
 
Emerging Technologies and the Clinical Trial Start-up
 
Emerging Trends in Patient Recruitment
 
Emerging Trends in Patient Recruitment: The Evolution of Clinical Science Liaisons into Patient Recruitment Support Conduits for Medical Device and Biopharmaceutical Sponsors
 
Engaging and Retaining Talent - How Critical is Personality?
 
Engaging the Community - Centralized Clinical Research Recruitment
 
Enhancing Site Performance with Project Management Techniques
 
Enhancing the Revenue Management Cycle for Sites
 
Enrolling and Retaining a Diverse Community-Based Population: Challenges and Strategies
 
Enrolling Critically Ill Children in Research: Opportunities and Challenges
 
Ensuring Quality Monitoring by Utilizing Auditing Techniques - NOT RECORDED
 
Ensuring Success Through Smarter Site Selection and Study Feasibility
 
Ensuring Success Through Smarter Site Selection and Study Feasibility
 
Ensuring Success When Implementing a Clinical Trial Management System (CTMS)
 
Establishing a Quality Control Program for Investigator-Initiated Studies
 
Ethical Considerations for the Informed Consent Process
 
Ethical Considerations in Patient Recruitment
 
Ethical Dilemmas in Clinical Research: A Case-Based Approach
 
Ethical Dilemmas: Expressions of Nurses' Grief
 
Ethical Issues in Research Management 2008
 
Ethical Mess-ups in Drug Development
There will be no slides for this session.
 
Ethical Research Hinges on the Risk/Benefit Relationship
 
Ethical Research Involving Children Hinges on the Risk Benefit Relationship
 
Ethics in Medicine and Research: Lessons from Dr. Mengele (Plenary Session)
 
EU Clinical Trials Regulation - Status Quo
 
EU Clinical Trials Regulation: Live in 2016?
 
Evaluating Hurdles to Conducting Clinical Trials in South Asia
 
Evaluating the Literature: Becoming a Functional Subject Matter Expert
 
Evaluation of Competence Ability among People with Schizophrenia on Consent Form
 
Evaluation of the National Institute of Allergy and Infectious Diseases (NIAID) Protocol Development Program - NOT RECORDED
 
Everything You Need to Know About FDA Warning Letters
 
Evidence-Based Feasibility Model: Leveraging Data to Inform Best Practice
 
Evolving Ethics of Animal Use Within the Clinical Research Enterprise
 
Evolving Medical Device Issues in the Industrialized Countries
 
Exception from Informed Consent (EFIC): Experiences from a Pediatric Trial
 
Exception to Informed Consent Regulation: Challenges and Successes in the Emergency Setting
 
Executing a Recruitment and Retention Plan that Delivers Results
 
Expand Your Reach: IIIBs - Registries/Observational Trials
 
Expanded Access of Unapproved Devices and Other Clinical Uses of Devices
 
Expanding Your Community Enrollment Networks
 
Explore Your Strengths and Put Them to Work: Getting Ahead as a Clinical Research Professional
 
Exploring Accreditation: The Value, Opportunities and Logistics of Establishing an Accreditation Program for Clinical Research Education
 
Exploring Patient and Physician Motivation for Participation in Large Simple Trials
 
Faces Behind the Regulations
 
Faces Behind the Regulations 2011
 
Facilitating Monitor Access to Electronic Health Records
 
Facilitating Remote Monitoring with a Paperless Clinical Trial Management System
 
Fail to Plan or Plan to Fail
 
Fast Track to Success for New Clinical Research Coordinators
 
Fast Track to Success for New Clinical Research Coordinators
 
FDA & Multimedia: Tools for Your Research
 
FDA & OHRP Update
 
FDA & OHRP Update
 
FDA as a Public Health Agency (Monday Plenary)
 
FDA as a Public Health Agency (Monday Plenary)
 
FDA Audits/Warning Letters
 
FDA Draft Guidance on Informed Consent: Wow Lets Discuss!
 
FDA Expectations for Investigator: Are You FDA Compliant?
 
FDA Final Guidance-Investigators: Medically Qualified Staff
 
FDA Guidance Documents in the Clinical Development Process
 
FDA Inspection in Device Clinical Trials: Taking Steps to Ensure Your Trial Succeeds
 
FDA Inspection of a New Drug Clinical Investigator: From A to Z
 
FDA Inspections: Handling the Consequences
 
FDA Inspections: Handling the Consequences (REPEAT)
 
FDA Inspections: Understand the Process and Manage the Consequences
 
FDA Inspections: What to Expect and How to Respond to Warning Letters
 
FDA Inspects the Site: Are You Ready?
 
FDA's Enforcement of a Clinical Investigator: Part 2
 
FDA-CDER: Three Topics from 2014 Conference Attendees
 
FDA-CDER: Three Topics from 2015 Conference Attendees
 
FDA/OHRP Update
 
FDA/OHRP Update
 
FDA/OHRP Update
 
FDASIA and FDA Guidelines on Race and Ethnicity Reporting: What You Need to Know
 
Filing an Investigator Initiated IND
 
Filling the Gaps: The Need for an Institutional CRC Network
 
Financial Conflict of Interest in Clinical Research
 
Financial Forecasting; Developing a Pro-forma for Your Site
 
Financial Management of the Clinical Research Program
 
First in Human (IDE) Studies with Devices in "Non-Traditional" Countries
 
First in Human Experience and Pivotal Studies
 
First in Human Trials--Warning--Be Careful at Your Site
 
Fit for Purpose: Design, Implement and Sustain the Right Quality Management System for Your Site
 
Fixing Feasibility - Addressing the Root Causes
 
Four Important Steps Researchers Should Take to Protect the Research Subject's Privacy
 
Fraud Enforcement in Clinical Research Under the False Claims Act
 
From PI to CRC: Training Your Clinical Research Staff
 
From Sinners to SAINTS: How One Academic Medical Center Created a Career Path and Cultural Home for Clinical Research Personnel
 
Frontiers of Clinical Trial Design
 
Future of Drug Regulation and Approval
 
GCP Compliance at Clinical Sites - Regulatory Differences
 
GCP Education Revolutionizes Clinical Research Conduction in Israel
 
GCP Inspection and Audit Readiness
 
Gender and Racial Disparity Among Clinical Investigators
 
Gene Expression Profiling in Clinical Trials Using Microarrays: Technology and Applications
 
Genetic Testing and the Enhancement Clinical Trial Design
 
Getting and Staying Ahead of the Game - Continuing Professional Development
 
Giving Your Studies a FAIR (Federal Regulations, Agreements, Investigational Plan, Requirements of IRB) Shake
 
Global Compliance with EU PV System Requirements
 
Global CRA Study Examining Workload and Time Utilization
 
Global GCP Issues - Confessions of an Auditor Road Warrior
 
Global Perspectives on the Informed Consent Process
 
Global Trial Planning - Determining the Optimum Mix of Countries and Sites
 
Global Virtual Teams: Benefits, Challenges and Best Practices for Effective Cross-Cultural Collaboration
 
Globalization of Clinical Research: Site Assessment and Management
 
Globalization of Clinical Research: Trends and Implications on the Clinical Trials Workforce
 
Globalizing Data Capture Through Scanning Technology
 
Good Clinical Practice (GCP) - Everything You Always Wanted to Know but Were Afraid to Ask! - NOT RECORDED
 
Got Research Billing Compliance?
 
Grand Opening: The Investigator Site: Before & After Pearls
 
Group Dynamics in Medical Device Project Teams
 
Guidance and Rule Updates on Unique Device Identification (UDI)
 
Guilty 'Til Proven Innocent: A Look at IRB Liability
 
Guilty Until Proven Innocent: A Look at IRB Liability
 
Guinea Pigs or Heroes? Conceptualizing the Relationship between Research Subjects and Investigators
 
Health Canada Guidance Documents as Compliance Tools
 
Health Literacy in Clinical Research
 
Healthcare 2019: Health, Technology, Value and the Opportunity for a Learning Health System (Plenary Opening Session)
 
Henrietta Lacks: A Discussion about Research Ethics and Social Responsibility
 
Hidden Risks with Risk-Based Monitoring
 
HIPAA & Clinical Trials: Fact & Fiction
 
Home Use Medical Devices and Usability Trials
 
Hospital Provider Challenges with Clinical Trial Billing
 
Hospital Site Selection: People, Place and Protocol
 
Hospital-Based Clinical Research Risk Management
 
How a Clinical Trial Liaison Can Make Enrollment and Study Compliance Successful at a Site
 
How Can I "Fix" My EHR to Support Research Operations, Part I
 
How Can I "Fix" My EHR to Support Research Operations, Part II
 
How Can My EHR System Better Support My Research Workflows? Part 1
 
How Can My EHR System Better Support My Research Workflows? Part 2
 
How Can Reports from EDC Systems Help in Clinical Operations
 
How Do IRBs Review Phase I Research? Considerations and Concerns in an Increasingly Global Community
 
How the FDA Guidance ?Protecting Rights, Safety and Welfare of Study Subjects ? Supervisory Responsibilities of Investigators? will Impact Clinical Sites
 
How to Become the Sponsor of Choice by Improving Relationships with Investigator Sites
 
How to Create a Subject Recruitment Website That Works
 
How to Improve Your Informed Consent? Learn from the FDA Guidance on Communicating Risk and Benefits!
 
How to Make FDA Inspections as Painless as Possible - What to Expect, What to Do and What Not to Do: A Site's Perspective
 
How to Make FDA Inspections as Painless as Possible: What to Expect, What to Do, and What Not to Do: A Site's Perspective
 
How to Prepare for an IRB Site Visit
 
How to Prepare Your Site For An IRB Compliance Audit
 
How to Run Investigator-Initiated Studies Compliantly
 
How to Seamlessly Transfer Your Study to Another IRB
 
How to Start and Grow a Business in Clinical Research
 
How to Successfully Conduct a Clinical Trial in the Emergency Room
 
How to Successfully Conduct International Device Feasibility Trials
 
How to Use Free Media to Increase Subject Enrollment
 
Human Clinical Research: A Historical Journey
 
Human Subject Protection: A View from the Bedside
 
Human Subject Protection: Cultural Sensitivity and Study Informed Consent Process in Rural Areas of China
 
Human Subjects Protection: Overview and Pitfalls to Avoid - NOT RECORDED
 
Humanitarian Use Devices: It's Not That Complicated!
 
I Am No Guinea Pig - I Am Empowered
 
I Think I Can: Ethical Considerations for the Cognitively Impaired
 
I'm a CRA/CRC - When Did I Become a Trainer?
 
ICH GCP Guidelines: Documenting Study Events
 
Identification and Ethical Reporting of Suspected Fraud or Misconduct
 
Identity Theft in Clinical Trials - A Case Study
 
Immortal Life of Henrietta Lacks and Beyond
 
Impact of Legislation Changes for Class 3 Medical Devices in the European Union
 
Impact of Select Variables on the Consenting Process: Part 2
 
Implementation of the Joint Task Force for Clinical Trial Competency Framework
 
Implementing Bench-to-Bedside Translational Research in the Community
 
Implementing Beneficence: Outcomes from a Multi-Trial Recruiting Model
 
Implementing FDA/OHRP Training Standards: Are You Compliant?
 
Implementing FDA/OHRP Training Standards: Are You Compliant?
 
Implementing Monitoring Escalation Programs
 
Implementing Site Level Quality Assurance and Quality Control
 
Improve Your Study Efficiency!
 
Improving Communication Between Researchers and Nurses Caring for Study Participants
 
Improving Communication Skills to Address the Barriers to Informed Consent
 
Improving Efficiency - Defined Metrics at the Site Level - NOT RECORDED
 
Improving Investigator Payments on Global Trials - CRO's View
 
Improving Performance Together - Better Study Management through Site and Sponsor Collaboration
 
Improving Phase I Study Management: Operational Strategies
 
Improving Quality and Compliance Through Effective SOP Development
 
In Light of This Event Should This Study Continue?
 
In-Patient Research in the United States: Meeting Human Subjects and JCAHO Regulations
 
Incorporating Bioinstrumental Assessments in Clinical Trials
 
Incorporating Compliance Requirements into a Web-based Clinical Trial
 
Increase Profits by Enhancing Site Research Budgets - NOT RECORDED
 
Increasing Predictable Site Enrollment Success
 
Increasing Predictable Site Enrollment Success
 
Increasing Predictable Site Enrollment Success
 
Individual vs. Community: Balancing Rights, Benefits & Risks
 
Industry Outlook - What all Industry Stakeholders Must Know
 
Inefficiencies & Improvement Opportunities in Investigative Site Regulatory Compliance Processes
 
Influences and Challenges of Patient Recruitment and Retention in Clinical Studies: Successes and Suggestions
 
Informed Consent ? Regulatory Requirements, Process Considerations, and Ongoing Dilemmas
 
Informed Consent: One Size Does Not Fit All
 
Informed Consent: Process or Document?
 
Informed Consent: Risk is in the Eye of the Beholder - Risk Perception and Communication in Clinical Trials
 
Innovation and Global Health
 
Innovations in Clinical Research Education
 
Innovative International Recruitment and Retention: Successful Planning and Implementation
 
Inpatient Trials: Study Awareness and Subject Evaluability
 
Inside the FDA: Drug Good Clinical Practice Regulations Compliance
 
Inspection Findings Related to the Informed Consent Procedure: Lessons Learned
 
Intellectual Property and FDA Regulated Products
 
Internal Audits & Risk Management for PI and Study Staff
 
International Research
 
Interpreting Clinical Regulations: Precautions and Warnings
 
Introducing the Newest InVitro Diagnostic: Computer Aided Detection (CAD)
 
Introduction to Imaging in Clinical Trials
 
Investigator Challenges Based on FDA Guidance Documents
 
Investigator Initiated Submission of IND/IDE Applications
 
Investigator, How May We Help You?
 
Investigator-Initiated Sponsored Research: Global Collaborations with Industry and Academia
 
Invited Presidential Symposium: Individualized Medicine and its Impact on Clinical Research
 
Is My Monitoring Adequate?
 
Is My Monitoring Adequate? Building Quality Into Your Monitoring System!
 
Is Risk-Based Monitoring a Risky Business?
 
Is Your Site Ready for Risk-Based Monitoring?
 
ISO 14155 - The GCP Equivalent for Medical Devices: Current Issues
 
It Doesn't Have to Hurt (Part 2): Really Having Fun Writing SOPs
 
It's Your Career: Own It!
 
It's in the Regs...or is it?
 
Item Writers
 
Joint APPI-PRIM&R Session: With the Best of Intentions: Has Regulation of Human Research Run Amuck?
 
Just the Facts Ma'am: Enrolling Patients Over Age 65
 
Keeping The Spark Alive During Long-Term, Multi-Center Trials
 
Keeping the Spark Alive During Long-Term, Multi-Center Trials
 
Key Concepts in IRB Review of Medical Device Studies
 
Keys to Great Source Documentation
 
Keys to Great Source Documentation
 
Keys to Writing Excellent Monitoring Reports and Follow-Up Letters
 
Knowledge is Power: The Importance of Training Everyone, from the Principal Investigators to the Hospital Administrators
 
La Sangre Latina: The New Force in Study Participation
 
Label-Driven Drug Development
 
Late Phase CRAs, A New Hybrid
 
Learning in the Digital World
 
Learning Objectives Met, But Was Practice Set? - NOT RECORDED
 
Left Out in the Cold? Review of Sample Storage Documentation - NOT RECORDED
 
Legally Effective Electronic Consent for Research - NOT RECORDED
 
Lessons From My Mother
 
Lessons in Vulnerability from Dickens' Christmas Carol
 
Lessons Learned: Loss of the PI
 
Lets Build Something Together! Using Centralized Services to Build and Run Clinical Research Studies (Examples from a CTSA Site)
 
Leveraging Procedure Consents to Enhance Subject Recruitment
 
Linking Education/Training with Personnel Certification for Clinical Research Professionals
 
Liposomes as Nanocarrier in Biomedical Research and Medicine
 
Local Lessons for Global Trials or Global Lessons for Local Trials?
 
Lost in Translation - Data Management for the Rest of Us
 
Making the Complex Compelling: Communicating Technical Information Effectively
 
Manage Your Career or Someone Else Will!
 
Manager as Chief Engagement Officer: Attract, Engage and Retain Your Critical Talent
 
Managing CRO Budgets: Models for Success
 
Managing Effective Medical Device Trials
 
Managing Risks and Quality in Outsourced Clinical Trials
 
Managing the Complexity Challenge: Research Site and Industry Perspectives on the Use of the Tool for Operational Protocol Scoring (TOPS)
 
Managing Time, Tasks and Relationships: Focusing on What Matters Most
 
Mapping and Navigating Your Career: How to Set Your GPS
 
Marketing and Public Relations for Your Clinical Research Practice
 
Marketing the Site to Increase Recruitment: A Coordinator's Perspective
 
Maximizing Productivity and Participant Welfare in Clinical Research
 
Maybe it Needs to Hurt a Little: Getting SOPs Done!
 
Measuring Effectiveness of Clinical Research Training
 
Measuring Performance: Metrics from a Site's Perspective
 
Medical Device Rescue Studies: Lessons Learned from Industry and CRO Perspectives
 
Medical Device Rescue Studies: One Year Later - Lessons Learned From Industry and CRO Perspectives
 
Medical Writing and Publication Planning in Clinical Research
 
Medicines Regulation - In the Right Direction? A Global Perspective
 
Meeting HIPAA & FDA Requirements for Case Histories
 
Meeting the Challenges of Clinical Trial Disclosure
 
Meeting the Cognitive Challenge of Informed Consent
 
Mentoring for Success in Clinical Research: Are You Prepared to be a Mentor?
 
Method to Success - How to Overcome Six Common Hurdles in Setting Up a Clinical Stem Cell Center
 
Metrics are Key to Success for Faster Clinical Trials
 
Metrics for Determining Clinical Trial Feasibility
 
Minimizing Institutional Risk: Oversight of IND/IDE Research
 
Mobile Technologies in Patient Engagement and Retention
 
Mobile Technology - Shifting the Landscape for Clinical Research Engagement: Case Studies and Discussion
 
Models of Clinical Research Performance in Academia
 
Modernizing FDA's Clinical Trials/BIMO Programs
 
Money in Medicine: Sin or Salvation?
 
Monitoring and Auditing Tools for Quality Research
 
Monitoring Electronic Records for Data Integrity
 
Monitoring for Quality: Risk-based Clinical Monitoring
 
Monitoring of Multinational Sites in a Principal Investigator (PI) Initiated Study - NOT RECORDED
 
Monitoring Versus Auditing Versus Inspections: Aren't They All the Same?
 
Multidisciplinary Interpretation of FDA Draft Guidance of Investigator Responsibilities
 
Multigenerational Learning: Do You Get Me Now?
 
Multitasking in Academia: Research, Education and Community
 
Mutual Feasibility - The Dance
 
Negative Aspects of a Hot Topic: Sample Size Re-Estimation
 
Negotiating the Contract Process
 
Negotiating the Contract Process
 
Negotiation of Clinical Study Agreements between Bio/Pharmaceutical Companies and Academic Medical Institutions
 
Next Steps, Right Steps: Exploring Career Choices in Clinical Research Industry Opportunities
 
NIH Support of a Single IRB Approach to Review Multicenter Clinical Research and Implications for Academic Centers
 
No More 'One Size Fits All' - A New Approach to Role-Based Training for Clinical Professionals
 
Not Your Usual Clinical Trial Training: Making Required Training Fun and Effective
 
Now What? A Review of Last Year's Major U.S. Events and What They Mean to Us
 
Nuremburg Code, Declaration of Helsinki, and Belmont Report
 
Observational Research: Areas of Consensus and Divergence
 
Observations of a Major Device Company on the Use of Fax-CRFs or E-CRFs: Are FAX-CRFs and E-CRFs Really Superior to Paper CRFs?
 
Office Emergency Preparedness for Clinical Trials
 
Office of Human Research Protections (OHRP) Guidance: Challenging Human Subject Protection Issues
 
OHRP/FDA Guidance on Reviewing and Reporting Adverse/Unanticipated Problems
 
One Clinical Trial, From a Global Perspective
 
One Size Fits All? Not for Small Sponsors and CROs
 
Opening Plenary Session: Partnerships in Human Subjects Research: Translating Genomic Discoveries to Clinical Medicine
 
Operational Excellence: Forecast & Balance Monitoring Demand
 
Opportunities & Challenges in Conducting Global Clinical Trials in India
 
Optimizing Clinical Research
 
Optimizing Communication Within Global Teams
 
Orphan Drugs and HDE
 
Other Duties as Assigned: Creating a Comprehensive Coordinator Training Program from A to Z
 
Outcomes Research
 
Outlook 2015: The Future Environment for R&D Part 1
 
Outsourcing Medical Device Trials: FDA & Industry Perspective
 
Overcoming the Challenges of Developing Site Rapport in a Post-Approval Study Setting
 
Overview of FDA Requirements for Humanitarian Use Devices
 
PALM Infrastructure Support Model for Enhanced Knowledge Management for Clinical Teams
 
Part 11 - Answers from Carbon, Silicon, or Nothing at All - NOT RECORDED
 
Partner Heresy: Redefining Sponsor-Provider Relationships - NOT RECORDED
 
Partnership for an Informed Subject: A Research Nurse's Perspective
 
Partnerships Between Army Research & University HRPP
 
Patient Recruitment for Sites: Beyond the Traditional Approach
 
Patient-Centric Medication with Direct-to-Patient Shipping
 
Patients Find Their Voice: A New Age of Informed Consent
 
Payment Terms and Their Effects on Cash Flow at the Site
 
Payment Terms in Clinical Trial Agreements and Their Effect on Cash Flow at the Site
 
Performance Evaluation Monitoring Visits: The Art of CRA Training and Assessments
 
Pharmaceutical Medicine Survey Results and Applications
 
Pharmacokinetics for the Non-kineticist: What Investigators, Coordinators, & Pharmacists Need to Know to Optimally Conduct Clinical Research
 
Pharmacokinetics for the Non-kineticist: What You Need to Know
 
Phase 0 Microdose Studies with Accelerator Mass Spectrometry as First in Human Trials - NOT RECORDED
 
Phase I Clinical Trials - Everything You Wanted to Know but Were Afraid to Ask
 
Phase I Oncology Clinical Trials: Site-Level Challenges and Solutions
 
Physician Payment Sunshine: A Ray of Hope or a Deeply Flawed Law?
 
PI Oversight: Making It Happen
 
PI Oversight: Making It Real
 
Ping Your Site: E-Media Strategy for a Solid Online Presence
 
Plan and Manage European Clinical Trials - Now the Regs - NOT RECORDED
 
Plenary #2 Monday
 
Plenary #3 Tuesday
 
Portal Technology: The Next Significant Innovation in Clinical Research
 
Post-hire Assessment and Competency Curriculum to Increase Performance
 
Poster Session P001/Collaboration With Other Departments to Maximize Enrollment/Create a High Performance CRA Team/Implementation of a CTMS Institution-wide
 
Poster Session P002/How Can You Mend a Broken Heart?: A Stem Cell Approach/IRB Guidelines: A Medical Device Research Perspective
 
Poster Session P003/Learning to Communicate in Multi-Disciplinary Teams
 
Poster Session P004/Disclosure of Trial Results to Research Participants/Measuring Consent Form Readability/Pediatric Assent: Key Factors for Forms and Procedures
 
Poster Session P005/Safety Reporting/The Secret to Successful Study Management
 
Poster Session P006/Regulatory and GCP Compliance in an International Setting/Where to Next: The Search for New Indication Opportunities
 
Poster Session P007/DNA of Successfully Managing Investigator-Initiated Trials/Site Activation Data from a Major Pre-Market Clinical Trial
 
Poster Session P008/Politics and Research: Third Party Pay to Play/Which Physicians are Seeing the Right Patient Types?
 
Poster Session P019:

Ethical Dilemmas of Dosing in One Country and Follow Up in Another Under ICH

All Aboard!: How Academic Medical Centers Can Succeed and Serve as Key Players in the Globalization of Clinical Research
 
Poster Session P033:

United States Medical Device Regulation

Dedicated Pharmacist Improves Function of Research Department
 
Poster Session P048:

The Management of a Clinical Research Program in a Large Academic Setting

Global Outlook: Survey of Study Coordinators on Global Patient Recruitment

Collecting Samples to Develop a Diagnostic Test: Flexible Study Design in a Changing Regulatory Environment
 
Poster Session P064:

A Clinical Research Coordinator Training Program that Produces Team Players
 
Poster Session P071:

Collaborating Study Sites Office

Regulatory Compliance of Institutionally Sponsored Investigator Initiated Human Subject Trials

Creating a Data Safety Monitoring Report Tracking System to Facilitate Regulatory Compliance

IRB Monitoring Program Improves Research Compliance
 
Poster Session P103:

An Informed Choice Model for Informed Consent: The Spine Patient Outcomes Research Trial (SPORT)

Ethical Considerations in Adherence Research
 
Poster Session P118:

Improving Enrollment in Acute MI Trials: Development and Education of the On-Call Research Nurse

Working with the Institutional Review Board Chair
 
Poster Session P146:

Creating a Collaborative Environment: Working Together at Monitoring Visits

Creatively Challenged? Visual Solutions to Your Patient Recruitment Advertising Problems

Direct-to-Consumer Activities Improve Study Recruitment Rates
 
Power of Human Potential: A Rare Disease Patient's Perspective
 
Practical Clinical Trials Model Program in Child Psychiatry (CAPTN)
 
Practical Considerations for GCP Audits in a Risk-Based Environment
 
Practical Ethics for Clinical Trials in Developing Countries
 
Practical Regulatory Compliance in Clinical Trials - NOT RECORDED
 
Practicing Good Science Through Ethical Study Design
 
Predicting Site Enrollment Using a Multiple Regression Model: An Investigation
 
Pregnancy Prevention During Trials: Beyond the Birds and the Bees
 
Premarket Notification (510(k))
 
Premarket Notification (510(k)) MDUFA III Changes
 
Premarket Notification (510(k)) Update
 
Premarket Notification (510(k)) Update
 
Premarket Notification 510(k) Update
 
Preventing Protocol Amendments: A Retrospective Analysis
 
Privacy in Research: PHI and the Advancement of Science
 
Proactive Patient Retention - Proactive vs. Reactive
 
Proactive Pharmacovigilance: Risk Management During Pre-Market Clinical Development
 
Progress and Programs Addressing Critical Needs for Professional Development: Outcomes
 
Project Managers Forum Session: Resource Your Clinical Project
 
Promise and Perils of Phase I Oncology Trials
 
Promoting Industry-Cooperative Group Collaborations: A Best Practice Approach
 
Protecting a Clinical Trial Participant's Interest in Clinical Research: An Indian Perspective
 
Protocol Development: How to Shorten the Long and Winding Road
 
Protocol Deviations: Writing, Reviewing and Reporting - What's Important and Why?
 
Protocol Feasibility – Make Your Research Study "Show" Ready
 
Quality Assurance Forum Session: Development of an Investigator Site QA System
 
Quality by Design (QbD): Simplified and Attainable
 
Quality by Design: The Value of CRF Mapping
 
Quality Data & High Enrollment Numbers: How to Get it All - NOT RECORDED
 
Quality Essentials: Monitoring Visit Report Review Plans
 
Quality Improvement: A Clinical Trials Investigative Site - NOT RECORDED
 
Quality Systems/SOPs: Creating a Path to Succeed
 
Quality Systems/SOPS: Creating Your Site's Path to Success
 
Quality Systems/SOPs: Keys to Success at the Site
 
Quantifying Beneficence in Evaluating Risks Versus Benefits
 
Query Wording - Hurling Words and Waiting for Echoes
 
Racial and Ethnic Minority Participation in Clinical Trials: Changing Misconceptions Into Solutions
 
Rare Disease Research Requires Consciousness, Commitment and Collaboration
 
RARE: The Journey of a Clinical Trial
 
Rating the Complexity of Individual Clinical Trial Tasks: A Comparative Analysis of Protocol Managers and Their Supervisors
 
Re-thinking Safety Assessment: An Integrated Solution from Day 1
 
REAL Face: Collaboratively Overcoming Barriers to Clinical Research Participation
 
Real-World Study Planning
 
Recognizing and Reporting Unanticipated Problems in Clinical Trials
 
Recruit to Retain: Mitigating Enrollment Risk Factors
 
Recruit to Retain: The Right Patients for the Right Reasons
 
Recruiting and Retaining Geriatric Patients: Strategies for Success
 
Recruitment Specialist: The Missing Link in Clinical Research
 
Recruitment Strategies for Special Population Studies
 
Reduced SDV, Web Portals, Audits ... Oh My!
 
Reducing Protocol Deviations - Integrated Quality Management
 
Reducing Trial Start-up and Recruitment Times in the United Kingdom (UK)
 
Registries and Post-marketing Safety Studies: Just Another Clinical Trial?
 
Regression Analysis: Techniques for Clinical Research
 
Regulatory Affairs Public Forum
 
Regulatory and Clinical Trial Management for IVD Studies
 
Regulatory and Ethical Considerations for Clinical Research Involving Mobile Technology
 
Regulatory and Ethical Considerations in Paying Physicians for Referring Patients to Clinical Trials
 
Regulatory and Ethical Issues in Healthcare's 'Big Data' Research
 
Relationship Building between Monitors and Coordinators
 
Remote Monitoring and Access to Electronic Medical Records
 
Remote Monitoring: How Far Can We Go?
 
Remote Monitoring: How Far Can We Go?
 
Removing the Barriers to Conducting Research in the UK NHS
 
Reporting Information on Falsification of Clinical Data
 
Reporting Unanticipated Problems: An IRB's Perspective
 
Requiring Good Clinical Practice Training for Investigators and Study Personnel
 
Research Billing Compliance for Dummies
 
Research Infrastructure to Maximize Efficiency
 
Research Liability & Data Management Under the Looking Glass ? When Process and Trends Matter
 
Research Registry Participants: Analyzing Behavior to Improve Enrollment Outcomes
 
Responding to GCP Inspection Findings - Follow-Up and Follow-Through
 
Response to FDA/OHRP Training Requirements: Update 2010
 
Results from the Joint Task Force Survey of Clinical Research Competence
 
Rethinking the Informed Consent Form
 
Reverse Engineering 483s and Warning Letters to Improve Your QA Program
 
Risk Based Monitoring: Implementation Methodology
 
Risk Benefits Management
 
Risk-Based Monitoring: Been There, Lived That, Thriving
 
Risk-Based Monitoring: Been There, Lived That, Thriving (REPEAT)
 
Risk-Based Monitoring: Multiple NIH-funded Protocols & Sites - NOT RECORDED
 
Risk-Based Monitoring: Right Sizing SDV Without Compromising Quality
 
Roadmap to Research: RN to CRA; RN to Study Coordinator
 
Roadmaps - A Tool for the Patient and the Research Staff
 
Roundtable: "Certification of Clinical Research Professionals - Pros and Cons"
 
Safety Culture in Clinical Research Organizations: What It Is
 
Secrets from the Front Lines: Patient Recruitment Insights, Best Practices and Biggest Challenges ? The Investigative Site Perspective
 
Self-Control Failure as a Trans-Disease Process
 
Serious Adverse Event (SAE) - Reporting in Class 3 Medical Device Trials in the European Union
 
Serious and Continuing Noncompliance: How IRBs and Sponsors Can Work Together to Manage Non-compliant Sites and Protect Human Subjects
 
Seven Mistakes Commonly Made During a Monitoring Visit - NOT RECORDED
 
Seven Steps to Establishing True Community Within a Clinical Trial
 
Shifting Paradigm Versus Reality of Risk-Based and Remote Monitoring
 
Should Academic Institutions Relinquish Review of Multi-Site Clinical Trials to Independent IRBs? The Pros and Cons
 
Should We Exploit Hope to Enhance Enrollment of Oncology Research Participants?
 
Site Managers Forum Session: Strategies in Human Resources as Solutions to Growing Companies
 
Site Performance Report Cards: What's Fair?
 
Site Selection - How Do You Do this Effectively in India
 
Site Visibility: How to Increase Visibility in Your Community
 
Site Visibility: How to Increase Visibility in Your Community
 
Site, IRB, Sponsor: Who Should Know What and When
 
Site, Sponsor, & IRB: Who Should Know What, When
 
SIVs vs. an Investigators Meeting: A Blended Approach
 
Six Smart Ways to Build Your Clinical Research Career
 
So You Have Been Chosen for an FDA Inspection: Guidance from a Former Auditor on How to Prepare, Host and Follow-Up for a Site Inspection
 
So You Have Been Chosen for an FDA Inspection: Guidance from a Former Auditor on How to Prepare, Host and Follow Up for a Site Inspection
 
So You Think You Know GCP...
 
So You Think You Know GCP...
 
So You Wanna Be a CRA?
 
So You Wanna Be a CRA?
 
So You Want To Be An Independent Consultant?
 
So You Want to be an Independent Consultant?
 
So, You Have Been Chosen for an FDA Inspection - Guidance from a Former Auditor
 
So, You Want to Be an Investigator: The Other Side of the Coin
 
Social Media in Clinical Trial Patient Recruitment
 
Social Responsibility and the Pharmaceutical Industry in the 21st Century (Sunday Plenary)
* There is no credits available for this session.
 
SOPs as Risk-Management Tools: Are Your SOPs Actually Increasing Risk of Non-Compliance?
 
Source Data Review (SDR) vs. Source Data Verification (SDV) - A Site Monitoring Best Practices Update
 
Special Concerns of Contraceptive and Reproductive Health Clinical Research
 
Special Considerations in Pediatric Trials for CRAs
 
Special Considerations when Working with Subjects in the Veteran Population
 
Special Considerations When Working With TBI, PTSD and SCI Subjects in the Veteran Population
 
Speed Drafting Your SOPs
 
Sponsor and Site Budget Development and Analysis: Effective Clinical Trial Budgeting
 
Sponsor and Site Budget Development and Analysis: Effective Clinical Trial Budgeting
 
Standardization, Collaboration and Technology: A Global Site and Industry Perspective
 
Standardizing PI Delegation Records
 
Standardizing Principal Investigator Delegation Records: An Alternative Approach for Sites
 
Standardizing Research Processes in Academic Institutions
 
Starting a New Research Site? Key Things to Know Before Opening the Doors
 
State Laws that Impact Good Clinical Practice: Focus on Informed Consent
 
Statistical Challenges Related to Protocol Noncompliance in Clinical Studies
 
Statistical Tests: So Many Choices, So Much Confusion
 
Statistical Tests: So Many Choices, So Much Confusion
 
Statistical Tests: So Many Choices, So Much Confusion
 
Statistics Premier
 
Stem Cell Tourism: An International Comparison
 
Strategic Site Partners - Getting From Here to There!
 
Strategies for Choosing Where to Conduct Your Device Clinical Study - U.S. or O.U.S.?
 
Strategies for Effective Recruitment and Retention in Clinical Studies
 
Strategies for Effective Use of GCP Testing of Researchers
 
Strategies for Improving Communication Between Sponsor and Site
 
Strategies for Patient Recruitment Management
 
Strategies for Writing Collaborative Scientific Papers - NOT RECORDED
 
Strategies to Build Quality Into Device Research
 
Strategies to Increase the Efficiency of Good Clinical Practice (GCP) Training: Recommendations From the Clinical Trials Transformation Initiative (CTTI)
 
Street Credibility: Using Word-of-Mouth Outreach to Recruit Special Populations for Your Study
 
Study Oversight Plans, Simplified
 
Study Selection: The Key to Site Success – Site and Sponsor Perspectives
 
Subject Enrollment: Some Sites Can and Some Don't--An Analysis of Thousands of Site Submissions will Uncover the Key Indicators to Success
 
Subject Recruiting: How Sites, Sponsors -- and Subjects -- Can Work Together
 
Subject Recruiting: The Missing Links
 
Subject-Centered ICF: A Research Nurse's Perspective
 
Success at the Crossroads: The Intersection of CDISC Standards with Research Site Processes
 
Successful Patient Recruitment and Retention in Europe
 
Successful Risk-Based Monitoring Implementation: Effective Strategies and Tactics for Your Organization
 
Successful Site Management of Drug Development Trends
 
Successfully Navigating the Clinical Research Landscape for Device Clinical Trials in Latin America
 
Supporting Enrollment & Engagement in Clinical Trials: SEEC - NOT RECORDED
 
Synergy in Collaboration: Data Management & Clin Ops
 
Taking the Mystery out of the Certification Exam
 
Taking the Mystery out of the Certification Exam
 
Taking the Mystery out of the Certification Exam
 
Taking the Mystery Out of the Certification Exam
 
Targeting the Untapped: Making it Easier to Reach Patients Over Age 65
 
Technical Data Review in IVD Studies
 
Techniques and Skills for Securing Compliance at the Clinical Investigator
 
Techniques for Brainstorming Effective Project Management Strategies for Major Project Scope Changes
 
The "Optimal Interim Monitoring Visit (IMV)": CRC and CRA Perspectives
 
The 10 Commandments of the Clinical Investigator
 
The 10 Reasons Your Recruiting Department is the Key to Your Success
 
The Battle of the Clinical Trial Agreements: Sponsor vs. Site
 
The Benefits of Integrated Marketing Programs
 
The Best Medicine: The Use of Humor in the Research Industry
 
The Best Medicine: The Use of Humor in the Research Industry
 
The Boundary Between Information and Promotion
 
The Brave New Regulatory World: Raising the Research Bar - NOT RECORDED
 
The Brave New World of Research Regulations: What You and Your IRB Need to Know Now
 
The British Columbia Clinical Trial Participation Survey
 
The Challenges of Implementing a New CTMS at a Large AMC
 
The Challenges of Infectious Disease Clinical Trials in Sub-Saharan Africa
 
The Challenges of Managing a Dual-Regulated Multi-Center Randomized Clinical Trial
 
The Changing Landscape of Medicare's Clinical Trial Coverage Policies for Medical Devices
 
The Changing Role of the Clinical Coordinator from Clinician to Computer Geek and Back Again
 
The Clinical Trial Transformation Initiative, An Update
 
The Clinical Trials Legislation in Europe: What Have We Learned ? What?s New?
 
The CRA's Role in Handling Investigator Non-Compliance
 
The CRA: Yesterday, Today and Tomorrow - NOT RECORDED
 
The Critical Role of Physicians in Increasing Diversity in Clinical Trials
 
The Crossroad: Clinical Research Career Development & Site Endorsement
 
The Culture of Safety and the Core Clinical Research Team: Investigators/Coordinators
 
The Current Situation of the Promotion of Clinical Trials in Japan
 
The Decision Science of Communicating Risks and Benefits
 
The Development of an Online Educational Academic-Industry Partnership in Clinical Recruitment Sciences
 
The Different Skill Sets of Clinical Research Coordinators - NOT RECORDED
 
The Fallibility of Feasibility: What We've Learned From Physicians
 
The Feasibility Frenzie
 
The Future of Training....Course Development for the 21st Century
 
The Genetic Information Non-Discrimination Act
 
The Identification and Development of Subject Matter Expert Trainers in Clinical Research
 
The Immortal Life of Henrietta Lacks: Applying Lessons Learned to Today's Informed Consent Process
 
The Impact of Health Care Reform on Clinical Research
 
The Impact of Risk-Based Monitoring on Clinical Research Sites
 
The Impact of Social Media Communities on Clinical Trials
 
The Importance of a Strong Study Feasibility Process, Accurate Site Selection and Patient Enrollment Strategy in India
 
The Independent CRA/CRC - Current Issues Facing the Independent Contractor
 
The Influence of 'Hope' on Oncology Research Participants and the Protection of Human Subjects
 
The Informed Consent Process - How Transparent is it in Developing Countries?
 
The Integral Role of a Research Lab Coordinator to Enhance the Efficiency of a Research Team
 
The Late Phase Safety Track
 
The Leaky Pipe Analysis - Validating Enrollment Potential for Your Site and Your Study
 
The Learn-Confirm Paradigm: Translation into Practice
 
The Metrics Evolution: Use Better Metrics to Improve Clinical Trials
 
The Mint Makes it First, It is Up to You to Make it Last: Effective Clinical Trial Budgeting
 
The Model Clinical Trials Office (CTO): Organization, Services and Start-Up Issues
 
The New eSource Draft Guidance - What Does it Mean to Me as a Site, CRA or Data Manager?
 
The New eSource Draft Guidance – What Does it Mean to Me as a Site, CRA or Data Manager?
 
The New World of Molecular Diagnostics in Cancer Clinical Trials - How Sponsors and IRBs Must Adapt
 
The Next Generation of Clinical Research: Developing Qualified Professionals
 
The Nitty-Gritty Details of Developing an Investigator-Initiated Research Protocol
 
The Nitty-Gritty of Data Collection and Reporting
 
The Nuts and Bolts of Adverse Events and What to Do With Them
 
The Nuts and Bolts of SOPs
 
The Process of Study Feasibility: Two Perspectives, One Common Goal
 
The Project Manager's Dilemma: Why Am I Too Busy to Manage My Project?
 
The Project Manager's Dilemma: Why am I Too Busy to Manage My Project?
 
The Pursuit of Hope and Dignity: Why Clinical Trials Matter to Patient
 
The Quality of Clinical Trials in China
 
The Role of Laboratory/ECG Findings in Subject Safety
 
The Science and Clinical Research Behind Consumer Products and Cosmetics
 
The Senior CRA: How to Earn Respect
 
The Site Activation & Subject Enrollment Critical Path
 
The Site Feasibility Survey: Ensuring a Successful Marriage Between a Site & Sponsor/CRO by Asking Tough Questions During the Dating Period
 
The Site Information Questionnaire: A Valuable Tool?
 
The Site Recruitment Specialist - Revisited
 
The Sponsor Request for Proposal and CRO Selection Process
 
The Times They are a Changin': Seven Key Regulatory Changes for Researchers and IRBs
 
The Top 10 Phase I, IIa Site Audit Findings and How Could These Have Been Prevented
 
The True Costs of Site Regulatory Compliance and Improvement Opportunities
 
The Unique Challenges of Comparative Effectiveness Research
 
The Use of Clinical Trial Data in Claims Support for Non-Rx Drug, Cosmetics, and Consumer Products
 
The Use of Placebos in Pediatrics
 
The Vulnerability of Children in Clinical Trials - Focus on the Indian Subcontinent
 
The Web of Relations: Thinking about Physicians and Patients
 
The Wizards of Oz
 
Three Perspectives: Conducting an Investigator-Initiated Multi-Center Clinical Trial
 
Three Ways Institutions Can Support Investigators Conducting Investigator-Initiated Research
 
Time for Change: Increased Investigator Responsibility
 
Tips and Tricks to Improve Your Workplace/Site
 
Top Five Pet Peeves - Impact, Management and Potential Solutions
 
Top Ten Things Sponsors/CROs Should Consider for Training of Clinical Sites
 
TOPS (Tool for Operational Protocol Scoring) - Site User Evaluation and Updates
 
Town Hall: Discussion on Site Marketing, Feasibility and Using Metrics
 
Town Hall: Interactive Discussion On Site Selection And Start-Up Implementation
 
Town Hall: Interactive Discussion On Site Selection And Start-Up Implementation (REPEAT)
 
Trainers Forum Session: Developing and Documenting "Adequate" Training
 
Training Across Generations
 
Training Podcasts
 
Training Your Research Team Members to Recognize Research Misconduct
 
Training, Standardizing, Correlating and Certifying Evaluators for Conducting Multi-Center Clinical Trials
 
Training: It is All About the Learner
 
Transferring Research Review and Oversight from One IRB to Another
 
Transforming the Conduct of Clinical Trials at an Academic Institution
 
Transitioning from CRC to CRA: Bridging the Gap
 
Translating Integrity and Compliance: International GCP Audits
 
Trends Related to Whistleblower Laws and Clinical Research and Trials
 
Trial and Error: Managing Research Liability Risks
 
Tribute to Dr. Felix Gyi: Research Ethics: Remembering the Past, Dealing with the Present and Preparing for the Future
 
Troubleshooting Trials - Lessons Learned from Rescuing Hundreds of Clinical Trials
 
Twitter and Patient Recruitment: Learn It, Use It & Track It
 
Twitter, Facebook, YouTube, Oh My! Patient Recruitment 2.0
 
Unanticipated Problems with Reporting Unanticipated Problems
 
Understanding AEs, ADEs, SAEs, and UADEs in Clinical Trials
 
Understanding and Navigating the Regulatory and Operating Environment in India Today
 
Understanding Clinical Trial Volunteer Experiences and Physician Referrals to Clinical Trials
 
Understanding International Perspectives in Pharmaceutical Medicine
 
Understanding IRBs: A Study of Their History and Development
 
Understanding Kaplan-Meier Methods for Non-Statisticians
 
Understanding Noncompliance: A Case Study Approach
 
Understanding P-Values for Non-Statisticians
 
Understanding the Academic Research Center: Pitfalls vs. Potential
 
Understanding the Epidemiologist's Role in Clinical Research
 
Unleash Healthcare Information Technology for Successful Sites, Investigators and Subjects
 
Unlocking the Positive Value of Ethics Using Educational Games
 
Update on Clinical Trials Regulatory Issues in India
 
Update on the Clinical Development Enterprise
 
Update on the FDA's Clinical Trials Transformation Initiative (CTTI): Implications for Clinical Monitoring and SAE Reporting
 
Updating Your Patient Recruitment Strategy: The Importance of Implementing Social Media and Online Campaigns
 
US Healthcare Reform's Continuing Impact on Our Industry
 
US Healthcare Reform's Continuing Impact on Our Industry
 
Use of Gamma Scintigraphy to Understand Inhaled Device/Formulation Variables on Delivery Efficiency and Deposition Profile for Systemic Therapies
 
Use of MedDRA for Coding in the Biopharmaceutical Industry ? Data INPUT Focused
 
Use of MedDRA for Data Retrieval and Presentation ? OUTPUT Focused
 
Use of Registries to Advance the Regulatory Science for Medical Devices
 
Use of Standard Operating Procedures to Streamline IRB Submissions
 
Using a Blended Approach to Clinical Research Training
 
Using a Central IRB in a Hospital Setting: A Real World Case Study of an ?Alternative Model? of IRB Review
 
Using a Data-Driven Approach with Sites During the Feasibility Process to Help Ensure a More Accurate and Successful Trial Outcome
 
Using an Electronic Site Visit Report to Streamline Visit Reporting
 
Using Clinical and Operational Data to Determine Optimal On-Site Visit Frequency
 
Using Communication Theory to Improve Informed Consent
 
Using Continuous Improvement Principles in Clinical Research
 
Using EHR Data and Herding Cats: One Data Center's Story
 
Using FDA Warning Letters as a Tool to Evaluate and Improve Your Research Activities at Clinical Sites
 
Using Gamification to Incentivize Sites
 
Using Medical Simulation in Protocol Design and Training
 
Using Open Source Technology and CDISC Standards to Enhance Clinical Trials
 
Using Personalized ePortfolios to Demonstrate Professional Competency in Clinical Research
 
Using PHR Platforms and Social Media for Patient Recruitment
 
Using Real World Data to Improve Site Feasibility and Recruitment in Clinical Trials of Rare Diseases
 
Using the Clinical Quality System Model in a Small Company
 
Utilization of Undergraduate Students as Research Assistants in Multiple Tertiary Care Emergency Departments and Intensive Care Units: Program Development and Success
 
Utilizing Soft Skills in Clinical Research
 
Vendor Oversight: How Sponsors Can Manage Their CRO Whilst the CRO Manages the Project
 
Viewing Human Subject Protection Issues from the Perspective of a Comprehensive Cancer Center
 
Virtual Investigational Device Exemption (IDE)
 
Vital Statistics: Understanding Basic Statistical Concepts
 
Voice of the Subject - Engaging the Public Regarding Their Participation in Research
 
Vulnerability: Do You Know It When You See It?
 
Vulnerability: What the Regulations Don't Say
 
Vulnerable Subjects - Do You Know One When You See One?
 
Walk the Talk: Implementing Risk-Based Monitoring
 
Walking Through The New Unified Code of Ethics for ACRP and APPI
 
Was Belmont Wrong? A Critical Look at Informed Consent Comprehension
 
We Have an Implantable Device Recall, What Next? Developing a "Playbook" for Managing Trials During Device Recalls or Safety Alerts
 
We Hold These Corrections to be Self-Evident
 
What "IS" Crucial: From Regulation to Meaningful Compliance
 
What "IS" Crucial: From Regulation to Meaningful Compliance
 
What are the Chances? Survival Probability Statistics - NOT RECORDED
 
What Do Sites Need? Training from the Site Perspective
 
What Does the FDA Really Say About Source Documentation? - NOT RECORDED
 
What Exactly Are You Asking? Comparing Genomic and Self-Reported Ancestry
 
What If...Business Continuity Planning for Clinical Trials - NOT RECORDED
 
What IS the Relationship Between an HDE (Humanitarian Device Exemption) and HUD (Humanitarian Use Device) or are They the Same?
 
What Motivates Clinical Investigators to Participate in Clinical Trials and Why are Some More Productive than Others?
 
What Should Investigators Know and How Should They Learn It?
 
What's New in Bioresearch Monitoring at FDA?
 
What's the Point? Therapeutic Misconception Among Research Practitioners
 
When and How to Best Use Media for Patient Recruitment
 
When Can Biomarkers Accelerate Drug Development? Breathing New Life Into an Old Question * There is no credits available for this session.
 
When Good Projects Go Bad
 
Where Do I Go From Here: Career Ladders for CRAs
 
Who Are Medical Writers and Why Should I Care?
 
Who Owns "Me"
 
Who Owns the Protocol?
 
Who's Watching Who? Investigator and IRB Compliance
 
Whose Responsibility is it... Really?
 
Why and How Academia Should be Running Clinical Trials
 
Why Should Your Investigator Site Be Chosen?
 
Why Webinars Don't Work and What You Can Do to Make Site Training More Engaging and Effective
 
Women as Subjects of Clinical Trials in the Indian Subcontinent
 
Work Smarter: Practical Tools to Improve Workflow
 
Working with Vulnerable Geriatric Subjects in the VA Population
 
Would You Become A Whistle Blower? Whistle Blowing in Clinical Research: The Price of Accountability
 
Wound Care and Clinical Research
 
Writing an Effective Corrective and Preventative Action (CAPA)
 
Yes You Can: Managing Recruitment Advertising Like a Pro
 
Yes You Can: Maximizing Your Ad Dollars
 
Yes! You Can Be a Better Monitor: Advanced Monitoring Techniques
 
You've Discovered Fraud - Now What Do You Do?
 
Your Site Doesn't Need 60 SOPs, But How Many Do You Need?
Browse All Speakers
 
Suheila Abdul-Karrim
 
Dorothy Abel
 
Solomon Abiola
 
Peter Adams
 
Amy Adams
 
Laurel Adams-Koss
 
Sherilyn Adcock
 
Maria Agcaoili
 
Neelum Aggarwal
 
Bob Albanese
 
Constance Albarracin
 
James Alderman
 
Charles Alexander
 
Christopher Allen
 
Albert Allen
 
Susan Allen
 
Amanda Alonso
 
Patricia Ames
 
Marty Anderson
 
Tammy Anderson
 
Sally Anderson
 
Diana Anderson
 
Leah Andrews
 
Jonathan Andrus
 
George Annas
 
Nicole Antinori
 
Donna Appell
 
Julia Appelt
 
Mitch Appleson
 
Harvey Arbit
 
Joe Archer
 
Richard Arlow
 
Sam Atkinson
 
Ronald Aung-Din
 
Hailey Austin
 
Dana Austin
 
John Avender
 
Sue Avery
 
Ali Azghani
 
Munther Baara
 
Veronica Baker
 
Alice Baker
 
Matt Baker
 
Naraida Balajonda
 
Leslie Ball
 
Soo Bang
 
Sudhakar Bangera
 
Alan Bank
 
Elizabeth Bankert
 
Michele Baptista
 
Chris Barkley
 
Mark Barnes
 
Jacqueline Barrows
 
Romiya Barry
 
Karen Bartels
 
Bryce Bartruff
 
Stacey Basham
 
Sarah Bass-Charlesworth
 
Eric Batten
 
Anne Marie Baughn
 
Anne-Marie Baughn
 
Kimberly Bazylewicz
 
Lea Becker
 
Julie Beckstrom
 
Ann Begley
 
Jamie Bell
 
Paul Below
 
Paul Below
 
Paul Below
 
Angela Belton
 
Cerdi Beltre
 
Stacey Bendele
 
Angela Benedetto
 
Angela Benedetto
 
Tim Benjamin
 
Brian Bennett
 
Karen Bennett
 
Sharon Benoit
 
Donna Benson
 
Jeffrey Berg
 
Annette Bernstein
 
Annette M. Bernstein
 
Annette Bernstein
 
Judy Bettencourt
 
Warren Bickel
 
Eryn Bilynsky
 
Theresa Bishop
 
Rene Blagg
 
Anne Blanchard
 
Anne Blanchard
 
Ann Blanchard
 
Kristina Blessing
 
David Bloomer
 
Deborah Board
 
Eleni Bobys
 
Joseph Bocchino
 
Elizabeth Bodi
 
Elizabeth Bodi
 
Heidi Boehm
 
Carol Bognar
 
Charlene Boisjolie
 
Wendy Boone
 
Wendy Boone
 
Luciana Borio
 
Leah Bouk
 
Dyana Boutwell
 
Scott Bradley
 
Derita Bran
 
Aleada Branch
 
Jeffrey Brandt
 
Donna Brassil
 
Alasdair Breckenridge
 
Jennifer Brennan
 
Corey Bridges
 
Debra Briggs
 
Denise Brigham
 
Shay Brill
 
Murray Brilliant
 
Susan Brink
 
Troy Brinkman
 
Maureen Brinkman
 
Maureen Brinkman
 
David Bristol
 
Russell Broaddus
 
Rick Brogden
 
Amber Brooks-Wolfe
 
Bridget Browder
 
Roger Brown
 
Betsy Brown
 
Betsy Brown
 
Stephen Brown
 
Allen Brown
 
Brittan Browning
 
Brittan Browning
 
Tanya Brubaker
 
Vanessa Bryant
 
Rebecca Budd
 
Thelma Bueno
 
Gary Bufferd
 
Fritz Buhler
 
Leigh Burgess
 
Jo Burmester
 
John Burnett
 
Jeri Burr
 
David Burrow
 
David Burrow
 
Valera Bussell
 
Quincy Byrdsong
 
Kelly Cahill
 
Kelly Cahill
 
Christopher Cain
 
Kelly Cairns
 
Kerri Cali
 
Sara Calvert
 
Nancy Calvin-Naylor
 
Joseph Camardo
 
Julie Campe
 
Christy Canady
 
J. Carbary
 
Claire Carbary
 
Rebecca Carew
 
Penelope Carlson
 
Karli Carpenter
 
Julie Carrico
 
Judy Carson-Gates
 
Elisa Cascade
 
Marilyn Cassell
 
Blanca Castillo
 
Michael Caswell
 
Patricia Cataruozolo
 
Connie Catha
 
Ruth Cavalieri
 
James Chamberlain
 
Peggy Chambers
 
Aaron Chan
 
Noel Chandler
 
Satish Chandra-Nair
 
David Chapin
 
Kim Chapman
 
Elizabeth Chase
 
Sandra Chase
 
Adam Chasse
 
Adam Chasse
 
Victor Chen
 
Victor Chen
 
Xiu Chen Yu
 
Savi Chetty-Tulsee
 
Richard Chin
 
Brandy Chittester
 
Hsien-Jane Chiu
 
Jill Christensen
 
Nikki Christison
 
Nikki Christison
 
Stephanie Christopher
 
Stephanie Christopher
 
Claudia Christy
 
Claudia Christy
 
Adam Chusid
 
Ann Marie Cisneros
 
Ann Marie Cisneros
 
Mary Clancy
 
Adele Clark
 
Eric Claude
 
Norbert Clemens
 
Norbert Clemens
 
Erin Clevenger
 
Celine Clive
 
Nicole Close
 
Chrissy Cochran
 
Jeffrey Cohen
 
Leigh Cohen
 
Leigh Cohen
 
Oren Cohen
 
Adam Cohen
 
Stanley Cohen
 
Jordan Cohen
 
Whit Coleman
 
Linda Coleman
 
Cal Collins
 
Stefan Comhaire
 
Peg Connelly
 
Scott Cooley
 
Kimberly Cooley
 
Jeffrey Cooper
 
Karena Cooper
 
Deborah Copeland
 
Philip Coran
 
Jack Corman
 
Peter Corr
 
Joseph Cosico
 
John Coundouris
 
Donna Cowan
 
Tara Cowell
 
Kelly Craig
 
Richard Craven
 
Kimberly Creekmur
 
Maureen Crocker
 
Denise Cunningham
 
Adam Cunningham
 
Jillyan Cunnup
 
Nicole Curry
 
Mary D'Rozario
 
Stacey DaCosta-Byfield
 
Esther Daemen
 
Esther Daemen
 
Laura Dalfonso
 
Valerie Danesh
 
Valerie Danesh
 
Saurendra Das
 
Paulla Davies
 
Diane Davies
 
Barbara Davis
 
Barbara Davis
 
Jennifer Davis
 
Yolanda Davis
 
J. Michael Dean
 
Juliette Dean
 
Patricia Degen
 
Sidney DeGraw
 
Christine Dehner
 
Mike Delahunty
 
Joy Delouth
 
Michel Denarie
 
Eslie Dennis
 
Paulla Dennis
 
Laura Denton
 
Ann DePaoli
 
Kayla Deru
 
Jean-Paul Deslypere
 
Paul Dewberry
 
Michelle Dickey
 
Kathy Dickinson
 
Eileen Dickman
 
Mary Ann DiLiberto
 
Kerri DiPietro
 
William Dirkes
 
Kathy Donato
 
Donna Dorozinsky
 
Kimberly Dorsch
 
Amy Doville
 
Diane Downs
 
Eleanore Doyle
 
Christine Drabick
 
Robert Dracker
 
Leah Drasher-Phillips
 
Alane Drexler
 
Deborah Driscoll
 
Deborah Driscoll
 
Michael Drues
 
Nancy Dubler
 
Stephanie Dubois
 
Michelle Duclos
 
Sharon Duffy
 
Roberta Duncan
 
Madeline Dunphy
 
Nancy Durham
 
Molly Dwyer-White
 
Maynard Dyson
 
Barb Early
 
Victoria Eaton
 
Christina Eberhart
 
Christina Eberhart
 
Tanya Eden
 
Donna Edgerton
 
Donna Edgerton
 
Tonya Edvalson
 
Jonnie Edwards
 
Tonya Eggleston
 
Carole Ehleben
 
Falk Ehmann
 
Jody Ehrhardt
 
Mohamed El Malt
 
Erica Elefant
 
Joanne Emmett
 
Melissa Enlow
 
Debra Ennis
 
Rene Enriquez
 
Rene Enriquez
 
Julie Erb
 
Lars-Olof Eriksson
 
Jeanine Estrada
 
Elizabeth Eyler-Pelletier
 
Rhonda Facile
 
Faculty
 
Laura Faden
 
Heather Fahs
 
Lindsey Fallenstein
 
Melissa Farrell
 
Jennifer Farrell
 
Erin Fassett
 
Andrea Favalora
 
Margaret (Peggy) Fay
 
Margaret Fay
 
Margaret Fay
 
Carol Fedor
 
Ellen Feigal
 
David Feigal
 
Michelle Feige
 
Sharon Feigenbaum
 
Olivia Feiro
 
Shantal Feltham
 
Ed Finerty
 
Gerald Finken
 
Baruch Fischhoff
 
Susan Fish
 
Susan Fish
 
Marian Fisher
 
Wendy Fisher
 
Wendy Fisher
 
Marisa Flanagan
 
Brigid Flanagan
 
Marie Fleisner
 
Kelly Flood
 
Kendra Ford
 
Kendra Ford
 
Kelly Forester
 
Judi Forman
 
Judi Forman
 
Judith Forman
 
Tina Forrister
 
Tina Forrister
 
Tina Forrister
 
David Forster
 
Draco Forte
 
Norman Fost
 
Stephanne Foster-Crane
 
Jean Fourcroy
 
Sarah Fowler-Dixon
 
David Fox
 
Sabrina Fox-Bosetti
 
Mindy Fraiser
 
Eunice Franklin-Becker
 
Marsha Amoy Fraser
 
Candida Fratazzi
 
Joy Frestedt
 
Joy Frestedt
 
Regina Freunscht
 
Yvonne Friedman
 
Trellis Frierson
 
Kristen Frino
 
Xin Fu
 
Edward Gabriele
 
Debra Gabrielson
 
Melissa Gaines
 
Christopher Gallen
 
Leo Galperin
 
Elisa Galvez
 
Karen Gammon
 
Janie Gardner
 
Megan Gardner
 
Elizabeth Garrard
 
Owen Garrick
 
Owen Garrick
 
Almenia Garvey
 
Almenia Garvey
 
Annie Garvey
 
Laidy Garzon
 
Kirstin Gatchalian
 
Cynthia Gates
 
Cindy Gates
 
Cynthia Gates
 
Sreekanth Gattu
 
Charu Gautam
 
Charu Gautam
 
Mary Gawlicki
 
Cami Gearhart
 
Adrian Gee
 
Pierre Geoffroy
 
Rita Gerard
 
Pierre Gervais
 
Kenneth Getz
 
Ken Getz
 
Kenneth A. Getz
 
Melynda Geurts
 
Yves Geysels
 
Anna Ghambaryan
 
Jan Gheuens
 
Philip Ghizoni
 
Ravindra Ghooi
 
Ale Gicqueau
 
Karen Gilbert
 
Karen Gilbert
 
Marianne Gildea
 
Joseph Giorgianni
 
Kate Giovino
 
Jiwan Giri
 
Joseph Giuliano
 
Barbara Gladson
 
Barbara Gladson
 
Kathy Godfrey
 
Sergio Ariel Godoy
 
Krista Goedel
 
Norman Goldfarb
 
Lyn Goldsmith
 
Lyn Goldsmith
 
Gretchen Goller
 
Carmen Gonzalez
 
Carmen Gonzalez
 
Lisette Gonzalez
 
Karen Gonzalez
 
Lisa Gordon
 
Bruce Gordon
 
Thomas Gorrie
 
Debbie Granner
 
Bob Greco
 
Jeanne Green
 
Paul Grossfeld
 
Glenda Guest
 
Glenda Guest
 
Leah Guidry
 
Tiffany Gunneman
 
Tiffany Gunneman
 
Suresh Gupta
 
Bill Gwinn
 
Felix Gyi
 
Felix Gyi
 
Janet Haas
 
Melissa Hagan
 
Yosuke Hagiwara
 
Bridget Hahm
 
Cynthia Hahn
 
Angelos Halaris
 
Sherita Hall
 
Deirdre Hall
 
Zachary Hallinan
 
Laurie Halloran
 
Laurie Halloran
 
Dave Hammond
 
Gerrit Hamre
 
Michael Hamrell
 
Michael Hamrell
 
Michael Hamrell
 
Michael Hamrell
 
Daniel Hand
 
Eileen Handberg
 
Amy Hanneman
 
Dan Harding
 
Matthew Harker
 
Joan Harley
 
Allecia Harley
 
Linda Harper
 
Beth Harper
 
Bradford Harris
 
Seneca Harrison
 
Michael Harte
 
Karen Hartman
 
Clare Hastings
 
Kim Hawkins
 
Karen Hedine
 
Clara Heering
 
Clara Heering
 
Mark Hegarty
 
Santosh Hegde
 
Jonathan Helfgott
 
Jean Hendrickson
 
Jean Hendrickson
 
Debra Henninger
 
Michel Hermans
 
Jennifer Herring
 
Jill Herring
 
Sara Hibbard
 
Donald Hiers
 
Jennifer Hill
 
Sandra Hines
 
Terri Hinkley
 
Terri Hinkley
 
Brigid Hobbs
 
Alan Hobson
 
Marcia Hodik
 
Marla Hoelle
 
Kelli Hoffman
 
Elizabeth Hohmann
 
Melissa Holbrook
 
Jennifer Holcomb
 
Jan Holladay Pierre
 
Debby Holmes
 
Donna Holmes
 
Janet Holwell
 
Feng Hong
 
Peter Honig
 
Lisa Horne Lucero
 
Tamara Hornyak
 
Stuart Horowitz
 
Stuart Horowitz
 
Diana Horton
 
Staci Horvath
 
Kit Howard
 
Christine Hoyer
 
Kathi Huddleston
 
Shannon Huffaker
 
Molly Huggins
 
Randall Huling
 
Ann Hummel
 
Hailee Hunt-Hawkins
 
Christine Hunter
 
Stori Hybbeneth
 
Michelle Hylan
 
Brent Ibata
 
Brent Ibata
 
Brent Ibata
 
Simon Ibell
 
Miyuki Inayoshi
 
Toshiko Ishibashi
 
Toshiko Ishibashi
 
John Isidor
 
Shauna Itri
 
Jeffree Itrich
 
Erin Iturriaga
 
M. Izzo
 
Christina Jackson
 
Susan Jackson
 
Cassie Jacobson
 
Jena Jankoski
 
Joseph Jankovic
 
Michael Jay
 
Elizabeth Jay
 
Michael Jay
 
Zhihong (Jenny) Jelsovsky
 
Michelle Jenkerson
 
Chris Jenkins
 
Emily Jenner
 
Danna Jennings
 
Ihn Sook Jeong
 
Marsha Johnson
 
Jane Marie Johnson
 
Todd Johnson
 
Ann Johnson
 
Otis Johnson
 
Marsha Johnson
 
Shelley Johnson
 
Shelley Johnson
 
Cynthia Joiner
 
Patricia Jones
 
Leslie Jones
 
Gary Jones
 
Martha Jones
 
Ryan Jones
 
Victor Jones
 
Karen Jones
 
Patricia Jones
 
Carolynn Jones
 
Rosie Jones
 
Paula Jones-Wright
 
Medha Joshi
 
Tanya Judkins-Cohn
 
Joy Jurnack
 
Joy Jurnack
 
Anita Kablinger
 
Anita Kablinger
 
Richard Kahn
 
Jeffery Kaine
 
Kenneth Kaitin
 
Dorina Kallogjeri
 
Becki Kanjirathinkal
 
Casey Kappenman
 
Patricia Karausky
 
Patricia Karausky
 
Patty Kasper
 
Patty Kasper
 
Dorothea Kasteleijn-Nolst-Trenite
 
Jennifer Kasztejna
 
Dori Kazimer
 
Levering Keely
 
Sheree Keever
 
Anna Keiper
 
Patrick Kelly
 
Timothy Kelly
 
Timothy Kelly
 
Terri Kelly
 
Paul Kelly
 
Terri Kelly
 
Ellen Kelso
 
Heather Kemp
 
Leslie Kemp
 
Leslie Kemp
 
Shawn Kennedy
 
Natalie Kennel
 
Valerie Kerr
 
Doug Kershaw
 
Gustavo Kesselring
 
Khalid Khan
 
Sharib Khan
 
Kai Kight
 
Joseph Kim
 
Andrew Kimball
 
Kathryn Kimmel
 
Kristina Kinard
 
Karen King
 
Bill King
 
Denise King
 
Gaye King
 
Jeff Kingsley
 
James Kirwin
 
Bron Kisler
 
Bron Kisler
 
Agnes Klein
 
Valma Klein
 
Conor Knightly
 
Deborah Kniuksta
 
Karol Knoop
 
Robert Kolb
 
Yuri Koo
 
Christine Korbmacher
 
Ahuva Koren
 
Michael Koren
 
Mark Koscin
 
Greg Koski
 
Paul Kosnik
 
Alexander Kostek
 
Judith Kramer
 
Holly Krasa
 
Joanne Krasnoff
 
Kenneth Kratz
 
Arlene Kray
 
Brooke Krininger
 
Pavel Kruchek
 
Cara Krulewitch
 
Raju Kucherlapati
 
Peter Kuijpers
 
Roxanne Kujanson
 
Vijai Kumar
 
Yuki Kuramochi
 
Deborah Kurtock
 
Rebecca Kush
 
Sheri Kuss
 
Hideo Kusuoka
 
Niki Kutac
 
Sandra Kweder
 
Shannon Labout
 
Denise Lacey
 
Denise Lacey
 
Jenny LaChance
 
Dennis LaCroix
 
Mark Lacy
 
Farynn Lagro
 
Lincy Lal
 
Tori Lallemont
 
Amy Lallier
 
Mary Jo Lamberti
 
Suzanne Lamerand
 
Julie Lamoureux
 
Tsuo-Hung Lan
 
Ronnie Landis
 
Jennifer Lansink
 
Jennifer Lanter
 
Caroline LaPlaca
 
Mario Laplume Garbarino
 
Debra Lappin
 
Patricia Larrabee
 
Kelly Larrabee
 
Valerie Larson
 
Deborah Lasher
 
Laurel Latto
 
Stephanie Lauenstein
 
Anne Laulederkind
 
Christina Ledbetter
 
Veronica Legg
 
Susan Leister
 
Diana Lenhardt
 
Jennifer Lentz
 
Michael Leon
 
Joanne Less
 
Matthew Lester
 
Matthew Lester
 
Lorena Levi
 
Daniel Levy
 
Susan Lewenz
 
Kristien Lewis
 
Janet Lewis
 
Janet Lewis
 
Lionel Lewis
 
Janet Lewis
 
Marcelo Lima
 
Josiana Limones Isenor
 
Josiana Limones-Isenor
 
Melody Lin
 
Marcy Lindley
 
Rebecca Little
 
Jenny Liu
 
Marlene Llopiz
 
Emily Lloyd
 
Barbara Lodico
 
Barbara LoDico
 
Tino LoSicco
 
Stephen Lovell
 
Catherine Lovett
 
Elizabeth Luoma
 
Lorenz Lutherer
 
Germaine Luyckx
 
Eric Lynam
 
Patricia MacCubbin
 
Patricia MacCubbin
 
Mark Macedo
 
Laurie Macleod
 
William Macneil
 
Michael Macri
 
Sandra Maddock
 
Kenneth Mahaffey
 
Terry Mainprize
 
Linda Malek
 
Sharleen Maley
 
Kerri Mallory
 
Almut Malone
 
Jennifer Maloney
 
Jennifer Maloney
 
Penelope Manasco
 
Laurin Mancour
 
Laurin Mancour
 
Edward Mannello
 
John Manolakis
 
Michael Marcarelli
 
John March
 
Danica Marinac-Dabic
 
Joyce Marinho
 
Jo-Mae Maris
 
Carol Marques
 
Jan Marshall-Campagnari
 
Shawna Martin
 
Fernando Martinez
 
Kate Marusina
 
Nicole Masen
 
James Mash
 
Sally Mashaly
 
Marcy J Maslov
 
Karen Massand
 
Tristan Massie
 
Tammy Massie
 
Tammi Masters
 
Tammi Masters
 
Yukiko Matsushima
 
Jill Matzat
 
Jill Matzat
 
Melissa Mau
 
Melissa Mau
 
Jennifer May
 
Jennifer May
 
April Mayberry
 
Jeffrey Mayhew
 
Don Mayne
 
Sean McAllister
 
Courtney McBean
 
John McBride
 
Mary McCabe
 
Katie McCarthy
 
Janine McCloskey
 
Yvonne McCracken
 
Yvonne McCracken
 
Michael McCrea
 
Darren McDaniel
 
Dan McDonald
 
Bruce McDonald
 
Bruce McDonald
 
Kim McDonald-Taylor
 
Alex McDonnell
 
Mattie McDowell
 
Michael McIvor
 
Kelly McKee
 
Barbara McKenzie
 
Angela McMahill
 
Angela McMahill
 
Jim McMillan
 
Lindsay McNair
 
Lindsay McNair
 
Kelley McNamara
 
Kara Lee McWatters
 
Alice Mead
 
Halia Melnyk
 
Cynthia Mendenhall
 
Patricia Mendoza
 
Jerry Menikoff
 
Sabrena Mervin-Blake
 
AnnMarie Mesick
 
Janet Messer
 
Cathy Metcalfe
 
Cathy Metcalfe
 
Cathy Metcalfe
 
Mark Metzner
 
Claire Meunier
 
Margo Michaels
 
Felix Michnacs
 
Jarrod Midboe
 
Sheila Mikhail
 
Sheila Mikhail
 
J. Stephen Mikita
 
Jamie Miller
 
Damon Miller
 
Daniel Miller
 
Lesley-Ann Miller
 
Jeffrey Miller
 
Tracey Miller
 
Jenifer Miller
 
Mary Mills
 
Sharon Minda
 
Meta Mitchell
 
Nada Mlinarevich
 
Farah Mompoint
 
Peter Monette
 
Kerry Moore
 
David Morin
 
Briggs Morrison
 
Richard Moscicki
 
Kathleen Mostek
 
Peter Motteram
 
Peter Motteram
 
Kirk Mousley
 
James Moyer
 
Eva Mozes-Kor
 
Susan Mozgai
 
Ann Mozo
 
Patricia Mozzicato
 
Subhendu Mukhopadhyay
 
Karen Mullin
 
Lisa Mullins
 
Lisa Mullins
 
Lisa Mullins
 
Dhinna Munshi
 
Leticia Murray
 
Sandra Mutolo
 
Pratibha Nadig
 
Noriaki Nagao
 
Nermina Nakas
 
Nermina Nakas
 
Madoka Nakayama
 
Prachi Nandoskar
 
Carl Naraynassamy
 
Robert Nauman
 
Irene Neaman
 
Katherine Needleman
 
Gerfried Nell
 
Kevin Nellis
 
Nadine Nemunaitis
 
Nadine Nemunaitis
 
Mark Neuberger
 
Jon Neville
 
Melissa Newman
 
Robert Newman
 
Robin Newman
 
Melissa Nezos
 
Chikako Nishimura
 
Cynthia Nolte
 
Tina Noonan
 
Lora Nordstrom
 
Kimberlly Nordstrom
 
Sharon-Lise Normand
 
Steve Norsted
 
Deborah Norton
 
Maria Nyakern
 
Ruth Ann Nylen
 
Robert O'Connor
 
Nicky O'Connor
 
Mikki O'Neal
 
P. Pearl O'Rourke
 
Susan Odum
 
Peter Odhiambo Ojwang'
 
Martin Olbrich
 
Kimberly Oleson
 
Axel Olsen
 
Axel Olsen
 
Russell Olson
 
Rachel Olson
 
Carol Opalek
 
Carol Opalek
 
Alison Orth
 
Madelene Ottosen
 
Madelene Ottosen
 
Al Pacino
 
Tricia Page
 
Rekha Pai
 
Sheryl Palmateer
 
Maria Palmer
 
Dannelle Palmer
 
Dannelle Palmer
 
Jim Pankovich
 
Darlene Panzitta
 
Paul Papagni
 
Paul Papagni
 
Catherine Parker
 
James Parmentier
 
James Parmentier
 
Diane Parrington
 
Mitchell Parrish
 
Adrian Parrott
 
Steven Pashko
 
Prathamesh Pathak
 
Peta-Anne Paul-Brent
 
Carla Pauley
 
Cindy Paulsen
 
Andrew Pavia
 
Stephanie Pawlak
 
Robert Pearsall
 
Carl Peck
 
Chester Pemberton
 
Barbara Pennington
 
Julie Pepe
 
Gualberto Perez
 
Jonathan Perlin
 
Kasia Petchel
 
Jan Peterson
 
Carolyn Peterson
 
Jill Petro
 
Jill Petro
 
JoAnn Pfeiffer
 
Michael Phillips
 
Constance Pickard
 
Charles Pierce
 
Charles Pierce
 
Christine Pierre
 
Christine Pierre
 
Cheryl Pikora
 
John Piletz
 
Ellen Pinnow
 
Ellen Pinnow
 
Mark Pinson
 
Cassandra Pitts
 
Kevin Pitts
 
Andrea Plati
 
Cecilia Plez
 
Michele Pliner
 
Michele Pliner
 
Vinod Podichetty
 
Ron Podraza
 
Wendy Portier
 
Karen Potter Jones
 
Deidra Poucher
 
Deidra Poucher
 
Deidra Poucher
 
Alicia Pouncey
 
James Powell
 
Lacey Powers
 
William Prather
 
Jenifer Prather
 
Amy Prechtl
 
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