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61 Results Found, Showing 1 - 50
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rating
1-1 - Signature Series Session -- A Conversation with the FDA 
Relevancy:
38.69% 
 
Date/Time:
April 29, 2017   8:15am - 9:30am
 
Format:
       
  Synced Audio / Video / Slides
 

 
2-2 - eSource as the Next Wave of Technology 
Relevancy:
45.85% 
 
Date/Time:
April 29, 2017   9:50am - 10:50am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
2-3 - Mastering Your Response to the Dreaded FDA Form 483 
Relevancy:
41.17% 
 
Date/Time:
April 29, 2017   9:50am - 10:50am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
5-1 - Lessons Learned: Preparing for a Successful FDA Advisory Committee Meeting 
Relevancy:
43.19% 
 
Date/Time:
April 29, 2017   3:45pm - 4:45pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
7-4 - Safety Reporting on Investigator-initiated Sponsored Research: It's Everyone's Job 
Relevancy:
40.18% 
 
Date/Time:
April 30, 2017   9:50am - 10:50am
 
Total Credits:
1.0 CH  
 
Speaker:
 
Format:
       
  Synced Audio / Video / Slides
 

 
7-6 - Regulatory Affairs Committee: 2016 Year-End Review and Looking Ahead 
Relevancy:
43.26% 
 
Date/Time:
April 30, 2017   9:50am - 10:50am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
9-2 - Clinical Evaluations of Safety and Risk 
Relevancy:
42.99% 
 
Date/Time:
April 30, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
W-4 - Practicing Good Science Through Ethical Study Design 
Relevancy:
41.40% 
 
Date/Time:
April 28, 2017   8:00am - 12:00pm
 
Total Credits:
3.5 CH  
 
Format:
 
  PDF Only
 

 
W-9 - Clinical Research Project Management: Essential Tools and Communication Strategies 
Relevancy:
44.37% 
 
Date/Time:
April 28, 2017   8:00am - 5:00pm
 
Total Credits:
7.0 CH  
 
Format:
 
  PDF Only
 

 
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10-1 - Evidence-based Analysis: The Path to Exceptional Clinical Research 
Relevancy:
74.83% 
 
Date/Time:
April 30, 2017   3:45pm - 4:45pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
11-5 - Trends, Strategies and Tools for Achieving Informed Consent 
Relevancy:
37.36% 
 
Date/Time:
May 1, 2017   8:30am - 9:30am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
12-5 - Build a Better Site Budget to Ensure Trial Success 
Relevancy:
44.75% 
 
Date/Time:
May 1, 2017   9:45am - 10:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
14-3 - Master Series Program Part I - Current CRU Issues in Planning and Executing Phase 1 Trials 
Relevancy:
59.28% 
 
Date/Time:
May 1, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
15-4 - Master Series Program, Part II — Current CRU Issues in Planning and Executing Phase 1 Trials 
Relevancy:
56.92% 
 
Date/Time:
May 1, 2017   3:45pm - 4:45pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
18-1 - Optimize Workflow and Resource Allocation Using LEAN-R 
Relevancy:
38.98% 
 
Date/Time:
May 2, 2017   11:00am - 12:00pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
1-2 - FDA Inspections: Understand the Process and Manage the Consequences 
Relevancy:
43.07% 
 
Date/Time:
April 16, 2016   9:00am - 10:30am
 
Total Credits:
1.5 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
1-7 - The Immortal Life of Henrietta Lacks: Applying Lessons Learned to Today's Informed Consent Process 
Relevancy:
34.40% 
 
Date/Time:
April 16, 2016   9:00am - 10:30am
 
Total Credits:
1.5 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
2-8 - Clinical Trial Study Management Plans: The Architecture of a Quality Clinical Trial 
Relevancy:
38.90% 
 
Date/Time:
April 16, 2016   2:30pm - 4:30pm
 
Total Credits:
2.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
2-9 - Rare Disease Research Requires Consciousness, Commitment and Collaboration 
Relevancy:
38.68% 
 
Date/Time:
April 16, 2016   2:30pm - 4:30pm
 
Total Credits:
2.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
3-9 - NIH Support of a Single IRB Approach to Review Multicenter Clinical Research and Implications for Academic Centers 
Relevancy:
93.16% 
 
Date/Time:
April 17, 2016   8:30am - 10:30am
 
Total Credits:
2.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
4-5 - Quality by Design: The Value of CRF Mapping 
Relevancy:
36.76% 
 
Date/Time:
April 17, 2016   10:45am - 11:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
4-7 - Collaboration in Patient-Centered Medical Device Innovation and Regulation 
Relevancy:
61.11% 
 
Date/Time:
April 17, 2016   10:45am - 11:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
7-1 - 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 
Relevancy:
65.29% 
 
Date/Time:
April 18, 2016   10:15am - 11:45am
 
Total Credits:
1.5 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
8-5 - Practicing Good Science Through Ethical Study Design 
Relevancy:
42.11% 
 
Date/Time:
April 18, 2016   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
8-7 - An Idea Whose Time Has Come: Next Steps in the Professionalization of Clinical Research 
Relevancy:
47.36% 
 
Date/Time:
April 18, 2016   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
8-8 - Learning in the Digital World 
Relevancy:
36.50% 
 
Date/Time:
April 18, 2016   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
9-1 - Cannabinoid Clinical Trials: Current Review, Problems, Pitfalls and Solutions 
Relevancy:
41.82% 
 
Date/Time:
April 18, 2016   3:45pm - 4:45pm
 
Total Credits:
1.0 CH  
 
Speaker:
 
Format:
       
  Synced Audio / Video / Slides
 

 
9-2 - Reverse Engineering 483s and Warning Letters to Improve Your QA Program 
Relevancy:
65.55% 
 
Date/Time:
April 18, 2016   3:45pm - 4:45pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
9-6 - Technical Data Review in IVD Studies 
Relevancy:
100.00% 
 
Date/Time:
April 18, 2016   3:45pm - 4:45pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
10-5 - Performance Evaluation Monitoring Visits: The Art of CRA Training and Assessments 
Relevancy:
38.62% 
 
Date/Time:
April 19, 2016   9:45am - 10:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
10-7 - Clinical Trial Agreements for Medical Device Sponsors 
Relevancy:
45.02% 
 
Date/Time:
April 19, 2016   9:45am - 10:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
11-1 - The Metrics Evolution: Use Better Metrics to Improve Clinical Trials 
Relevancy:
44.10% 
 
Date/Time:
April 19, 2016   11:00am - 12:00pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
11-2 - The Impact of Social Media Communities on Clinical Trials 
Relevancy:
40.00% 
 
Date/Time:
April 19, 2016   11:00am - 12:00pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
11-5 - Improving Communication Between Researchers and Nurses Caring for Study Participants 
Relevancy:
37.95% 
 
Date/Time:
April 19, 2016   11:00am - 12:00pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
11-9 - Subject-Centered ICF: A Research Nurse's Perspective 
Relevancy:
40.56% 
 
Date/Time:
April 19, 2016   11:00am - 12:00pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
Keynote 3 - "An Aerial View of Forces Reshaping the Global Clinical Research Enterprise" Keynote Presentation with Ken Getz 
Relevancy:
25.53% 
 
Date/Time:
April 18, 2016   7:15am - 8:15am
 
Total Credits:
1.0 CH  
 
Speaker:
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
S202 - Top Ten Things Sponsors/CROs Should Consider for Training of Clinical Sites 
Relevancy:
45.63% 
 
Date/Time:
April 25, 2015   2:45pm - 3:45pm
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
S304 - The New World of Molecular Diagnostics in Cancer Clinical Trials - How Sponsors and IRBs Must Adapt 
Relevancy:
37.38% 
 
Date/Time:
April 25, 2015   4:00pm - 5:00pm
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
S305 - Beam Me the Data Scotty! Site Monitoring Without the Plane 
Relevancy:
55.98% 
 
Date/Time:
April 25, 2015   4:00pm - 5:00pm
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
S501 - Inefficiencies & Improvement Opportunities in Investigative Site Regulatory Compliance Processes 
Relevancy:
40.89% 
 
Date/Time:
April 26, 2015   2:45pm - 3:45pm
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
S502 - Use of Standard Operating Procedures to Streamline IRB Submissions 
Relevancy:
41.28% 
 
Date/Time:
April 26, 2015   2:45pm - 3:45pm
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
S505 - Avoiding the Leap from 483 to Warning Letter - Lessons Learned 
Relevancy:
40.18% 
 
Date/Time:
April 26, 2015   2:45pm - 3:45pm
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
S605 - 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 
Relevancy:
66.63% 
 
Date/Time:
April 26, 2015   4:00pm - 5:00pm
 
Format:
       
  Synced Audio / Video / Slides
 

 
S703 - How to Seamlessly Transfer Your Study to Another IRB 
Relevancy:
44.15% 
 
Date/Time:
April 27, 2015   8:30am - 9:30am
 
Format:
       
  Synced Audio / Video / Slides
 

 
S706 - CTTI Use of Central IRBs for Multicenter Clinical Trials 
Relevancy:
68.37% 
 
Date/Time:
April 27, 2015   8:30am - 9:30am
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
S801 - An Update on Advances in Clinical Research on Sport-related Concussion 
Relevancy:
65.83% 
 
Date/Time:
April 27, 2015   9:45am - 10:45am
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
S802 - Source Data Review (SDR) vs. Source Data Verification (SDV) - A Site Monitoring Best Practices Update 
Relevancy:
81.91% 
 
Date/Time:
April 27, 2015   9:45am - 10:45am
 
Format:
       
  Synced Audio / Video / Slides
 

 
S908 - Strategies to Increase the Efficiency of Good Clinical Practice (GCP) Training: Recommendations From the Clinical Trials Transformation Initiative (CTTI) 
Relevancy:
40.84% 
 
Date/Time:
April 27, 2015   11:00am - 12:00pm
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
EL109 - FDA Inspections: Handling the Consequences 
Relevancy:
46.16% 
 
Date/Time:
April 25, 2015   8:30am - 10:30am
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
PS103 - Walk the Talk: Implementing Risk-Based Monitoring 
Relevancy:
37.93% 
 
Date/Time:
April 25, 2015   8:30am - 10:30am
 
Format:
       
  Synced Audio / Video / Slides
 

 
61 Results Found, Showing 1 - 50
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