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Association of Clinical Research Professionals

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ACRP 2015 Global Conference & Exhibition
ACRP 2016 Meeting & Expo
ACRP 2017 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
2017 Update: U.S. Healthcare Regulatory Changes and Their Impact on Clinical Research
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 Novel Approach: Using an Online Patient Community to Develop a PRO Instrument
A Quick Guide to Managing and Monitoring IVD Studies
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
ACRP Certification Exam Preparation Course
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
Attaining the Perfect Balance: Objective Protocol Feasibility Scoring
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
Battle of the Clinical Trial Agreements: Sites vs. Sponsors
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
Beyond Audit Survival: The Busy Clinical Research Professional's Guide To Audit Preparation
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
Blowing the Whistle: A 2017 Update on Fraud, Waste and Abuse 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
Breaches in Research Integrity: Maintaining the Public's Trust and Confidence
Breaker, Breaker 1-9: Effective Communication Strategies - NOT RECORDED
Bridging the Gap: Improving Communications Between Clinical Operations and Data Management
Bring Your Own Device: Is It Right for Your Clinical Research Enterprise?
Build a Better Site Budget to Ensure Trial Success
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
Capturing High-value Metrics that Drive Clinical Research Performance
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!
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 Evaluations of Safety and Risk
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 Research Project Management: Essential Tools and Communication Strategies
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
Coming in 2018! Get Ready for the New EU Medical Device 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
Core Competencies in Clinical Research: An Analysis of International Differences in Perceptions and Relevance
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 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 Managers: The Frontline Defense of Trial Risk Management
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
eConsent: Preparing for Paperless Consent
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 Strategies to Drive Program Success
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
Electronic Records, eSource Data and eConsent – Clinical Investigations and Regulatory Expectations
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)
eSource as the Next Wave of Technology
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 Analysis: The Path to Exceptional Clinical Research
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
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
Fine-tuning Your Vulnerability Radar
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
Forging a New Path to Professionalism: GCP vs. Core Competency-based Training
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 Auditing: Apply Your New Skills at Work
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
Hands Across the Water: A Comparison of Clinical Trials in the EU and U.S.
Harmonized Core Competencies for Monitors: A New Framework for Measuring Performance
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 Create, Structure and Implement a Mentoring Program Within Your Clinical Research Organization or Practice
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
Insights on Effective Communication and Outreach Among Patients and Advocacy Groups
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 Attrition: Strategies to Turn the Tide
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
Key Considerations in Building Your Site's Quality Improvement Program
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
Layperson Summaries: Should the U.S. Follow the EU Regulation?
Lead and Succeed in Your Clinical Research Team
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
Lessons Learned: Moving to Regulatory and Source eBinders
Lessons Learned: Preparing for a Successful FDA Advisory Committee Meeting
Let's Get Clinical! A Clinical Research Boot Camp
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 Business Intelligence the Cornerstone of Your Study Improvement Process
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
Master Series Program Part I - Current CRU Issues in Planning and Executing Phase 1 Trials
Master Series Program, Part I — Dramatization of the Informed Consent Process: Good Theater or Bad?
Master Series Program, Part I — Ethical Challenges in Pediatric Research
Master Series Program, Part I — Going Paperless: A Smart Way to Increase Site Efficiency and Save Resources
Master Series Program, Part I — The ICH GCP E6 R2 Revisions: Impact On The PI And Site
Master Series Program, Part I — The Quality Risk Management Plan: The Key to a Quality Trial
Master Series Program, Part I -- Clinical Research Finance & Billing: Are You Leaving Money on the Table?
Master Series Program, Part I -- Mastering the Art of Writing Monitoring Reports
Master Series Program, Part II — Current CRU Issues in Planning and Executing Phase 1 Trials
Master Series Program, Part II — Dramatization of the Informed Consent Process: Good Theater or Bad?
Master Series Program, Part II — Going Paperless: A Smart Way to Increase Site Efficiency and Save Resources
Master Series Program, Part II — The ICH GCP E6 R2 Revisions: : Impact On The PI And Site!
Master Series Program, Part II — The Quality Risk Management Plan: The Key to a Quality Trial
Master Series Program, Part II -- Clinical Research Finance & Billing: Are You Leaving Money on the Table?
Master Series Program, Part II -- Ethical Challenges in Pediatric Research
Master Series Program, Part II -- Mastering the Art of Writing Monitoring Reports
Mastering Your Response to the Dreaded FDA Form 483
Maximizing Productivity and Participant Welfare in Clinical Research
Maximizing the ROI of Your Clinical Trial Management System
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 Cannabis: A Substitute for Prescription Opioid Use?
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
Melding Consumer Big Data with Medical Big Data: The Regulatory and Ethical Implications
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?
Obtaining Consent in Acute Settings
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
Optimize Workflow and Resource Allocation Using LEAN-R
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
Phage Therapy: The Answer to Antibiotic Resistence?
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
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
Putting Patient-Centric Principles into Practice
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 Committee: 2016 Year-End Review and Looking Ahead
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
Returning Research Test Results: Know Your Ethical and Legal Obligations
Reverse Engineering 483s and Warning Letters to Improve Your QA Program
Revitalizing a Workforce: Aligning Job Classifications with Competencies
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
Safety Reporting on Investigator-initiated Sponsored Research: It's Everyone's Job
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?
Signature Series Session -- A Conversation with the FDA
Signature Series Session -- Innovating Clinical Trials with Mobile Technology
Signature Series Session -- Living with Eyes Wide Open
Signature Series Session -- The State of the Industry
Signature Series Session -- When the Physician Becomes the Patient: The Inspiring Story of Dr. Keith Eaton
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 2016 Medical Device Directive: What It Means to You
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 Evolving Clinical Research Enterprise: What Recent Legal and Regulatory Changes Mean to You
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 Power and Reach of Social Media in Clinical Trials
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 Science of Site Management: Using Metrics to Guide Decisions
The Seismic Shift in the Monitoring Paradigm: From Quality Control to Quality Assurance
The Senior CRA: How to Earn Respect
The Shared Investigator Platform: Revolutionizing Communication Between Sites and Sponsors
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 Social Media Blueprint: Tips for New Patient Advocacy & Recruitment
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
Tools to Help Clinical Sites Optimize Performance and Maintain GCP Compliance
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
Trends, Strategies and Tools for Achieving Informed Consent
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
U.S.-based IRBs vs. European and Latin American Ethics Committees
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
Unlocking the 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
Wearables and Big Data: The New Gold Standard for Clinical Trials
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 That You Say? When Research Subjects Struggle to Hear
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?
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Joy Jurnack
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Patricia Karausky
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Paul Kelly
Terri Kelly
Patrick Kelly
Timothy Kelly
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Heather Kemp
Leslie Kemp
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Gaye King
Karen King
Bill King
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James Kirwin
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Bron Kisler
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Yuki Kuramochi
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Denise Lacey
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Julie Lamoureux
Tsuo-Hung Lan
Ronnie Landis
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Jennifer Lanter
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Mario Laplume Garbarino
Debra Lappin
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Patricia Larrabee
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Anne Laulederkind
Derek Lawrence
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Christina Ledbetter
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Matthew Lester
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Janet Lewis
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Janet Lewis
Isaac Lidsky
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
Leanne Madre
Kenneth Mahaffey
Terry Mainprize
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Sharleen Maley
Kerri Mallory
Almut Malone
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Jennifer Maloney
Penelope Manasco
Laurin Mancour
Laurin Mancour
Edward Mannello
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John March
Danica Marinac-Dabic
Joyce Marinho
Jo-Mae Maris
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Ana Marquez
Jan Marshall-Campagnari
Shawna Martin
Fernando Martinez
Kate Marusina
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Tammi Masters
Yukiko Matsushima
Jill Matzat
Jill Matzat
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Melissa Mau
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Jennifer May
April Mayberry
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Don Mayne
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Yvonne McCracken
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Dan McDonald
Bruce McDonald
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Angela McMahill
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Lindsay McNair
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Jerry Menikoff
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Anab Mohamed
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Peter Monette
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David Morin
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Richard Moscicki
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Peter Motteram
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James Moyer
Eva Mozes-Kor
Susan Mozgai
Ann Mozo
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Subhendu Mukhopadhyay
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Lisa Mullins
Lisa Mullins
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Pratibha Nadig
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Ritsuko Nagasaka
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Nermina Nakas
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Khady Ndour
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Gerfried Nell
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Nadine Nemunaitis
Mark Neuberger
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Melissa Newman
Robert Newman
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Raymond Nomizu
Tina Noonan
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Kimberlly Nordstrom
Sharon-Lise Normand
Steve Norsted
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Peter Odhiambo Ojwang'
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Axel Olsen
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Rachel Olson
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Carol Opalek
Alison Orth
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Madelene Ottosen
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Dannelle Palmer
Jim Pankovich
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Paul Papagni
Paul Papagni
Catherine Parker
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James Parmentier
Diane Parrington
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Adrian Parrott
Steven Pashko
Prathamesh Pathak
Peta-Anne Paul-Brent
Carla Pauley
Cindy Paulsen
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Robert Pearsall
Carl Peck
Chester Pemberton
Barbara Pennington
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Gualberto Perez
Jonathan Perlin
Kasia Petchel
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Jan Peterson
Jill Petro
Jill Petro
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Douglas Pham
Michael Phillips
Constance Pickard
Charles Pierce
Charles Pierce
Christine Pierre
Christine Pierre
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John Piletz
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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
Jenifer Prather
William Prather
Amy Prechtl
Ernest Prentice
Ernest Prentice
Gil Price
Ivor Pritchard
Kevin Prohaska
Amber Purkeypile
Amber Purkeypile
Osman Qamar
Jenny Qin
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Sabrina Ramkellawan
Jeannine Ramsey
Jennifer Rankin
Hani Rashed
Stephen Raskin
Charles Rathmann
Sheri Rawlings
Daniel Redline
David Reed
Ronald Reed
Karen Reese
Rona Margaret Relova
Badri Rengarajan
Sherry Reuter
Linda Rhea
Linda Rhea
Zack Rhoades
Zack Rhoades
Stephen Rhodes
Angela Ricci
Karen Richey
Katie Richter
James Riddle
Michelle Ringdahl
Mary Elizabeth Ritchey
Sonia Robazetti
Karen Roberts
Susan Roberts
Jenene Roberts
Richard Robinson
Angi Robinson
Eileen Robinson
Laura Robison
Cheryl Roche-Alexander
Susan Rockwell
Susan Rockwell
Susan Rockwell
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