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81 Results Found, Showing 1 - 50
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rating
4-1 - eConsent: Preparing for Paperless Consent 
Relevancy:
30.63% 
 
Date/Time:
April 29, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
4-6 - Coming in 2018! Get Ready for the New EU Medical Device Regulation 
Relevancy:
63.66% 
 
Date/Time:
April 29, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
4-7 - Master Series Program, Part I — Going Paperless: A Smart Way to Increase Site Efficiency and Save Resources 
Relevancy:
27.85% 
 
Date/Time:
April 29, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 

 
rating
5-3 - Master Series Program, Part II — Going Paperless: A Smart Way to Increase Site Efficiency and Save Resources 
Relevancy:
27.85% 
 
Date/Time:
April 29, 2017   3:45pm - 4:45pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
7-6 - Regulatory Affairs Committee: 2016 Year-End Review and Looking Ahead 
Relevancy:
100.00% 
 
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:
33.74% 
 
Date/Time:
April 30, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
9-3 - Electronic Records, eSource Data and eConsent – Clinical Investigations and Regulatory Expectations 
Relevancy:
68.81% 
 
Date/Time:
April 30, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
9-4 - Master Series Program, Part I — Ethical Challenges in Pediatric Research 
Relevancy:
41.84% 
 
Date/Time:
April 30, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
W-1 - Tools to Help Clinical Sites Optimize Performance and Maintain GCP Compliance 
Relevancy:
33.33% 
 
Date/Time:
April 28, 2017   8:00am - 5:00pm
 
Total Credits:
7.0 CH  
 
Format:
 
  PDF Only
 

 
rating
W-2 - Let's Get Clinical! A Clinical Research Boot Camp 
Relevancy:
31.80% 
 
Date/Time:
April 28, 2017   8:00am - 5:00pm
 
Total Credits:
7.0 CH  
 
Format:
 
  PDF Only
 

 
rating
W-3 - GCP Auditing: Apply Your New Skills at Work 
Relevancy:
33.64% 
 
Date/Time:
April 28, 2017   8:00am - 5:00pm
 
Total Credits:
7.0 CH  
 
Format:
 
  PDF Only
 

 
W-5 - Hands Across the Water: A Comparison of Clinical Trials in the EU and U.S. 
Relevancy:
76.58% 
 
Date/Time:
April 28, 2017   8:00am - 12:00pm
 
Total Credits:
3.5 CH  
 
Format:
 
  PDF Only
 

 
10-3 - Master Series Program, Part II -- Ethical Challenges in Pediatric Research 
Relevancy:
42.69% 
 
Date/Time:
April 30, 2017   3:45pm - 4:45pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
10-6 - Melding Consumer Big Data with Medical Big Data: The Regulatory and Ethical Implications 
Relevancy:
57.92% 
 
Date/Time:
April 30, 2017   3:45pm - 4:45pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
11-2 - The 2016 Medical Device Directive: What It Means to You 
Relevancy:
51.43% 
 
Date/Time:
May 1, 2017   8:30am - 9:30am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
11-4 - Master Series Program, Part I — The Quality Risk Management Plan: The Key to a Quality Trial 
Relevancy:
26.30% 
 
Date/Time:
May 1, 2017   8:30am - 9:30am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
12-1 - CDER BIMO Compliance and Enforcement: What You Need to Know! 
Relevancy:
33.80% 
 
Date/Time:
May 1, 2017   9:45am - 10:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
12-3 - Master Series Program, Part II — The Quality Risk Management Plan: The Key to a Quality Trial 
Relevancy:
25.86% 
 
Date/Time:
May 1, 2017   9:45am - 10:45am
 
Total Credits:
1.0 CH  
 

 
rating
13-1 - Signature Series Session -- Innovating Clinical Trials with Mobile Technology 
Relevancy:
63.96% 
 
Date/Time:
May 1, 2017   11:00am - 12:00pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
14-1 - Key Considerations in Building Your Site's Quality Improvement Program 
Relevancy:
33.46% 
 
Date/Time:
May 1, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
14-2 - 2017 Update: U.S. Healthcare Regulatory Changes and Their Impact on Clinical Research 
Relevancy:
37.37% 
 
Date/Time:
May 1, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
14-4 - Master Series Program, Part I -- Mastering the Art of Writing Monitoring Reports 
Relevancy:
26.61% 
 
Date/Time:
May 1, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
15-5 - A Quick Guide to Managing and Monitoring IVD Studies 
Relevancy:
36.23% 
 
Date/Time:
May 1, 2017   3:45pm - 4:45pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
15-7 - Master Series Program, Part II -- Mastering the Art of Writing Monitoring Reports 
Relevancy:
25.82% 
 
Date/Time:
May 1, 2017   3:45pm - 4:45pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
17-1 - Obtaining Consent in Acute Settings 
Relevancy:
30.57% 
 
Date/Time:
May 2, 2017   9:45am - 10:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
17-2 - Lessons Learned: Moving to Regulatory and Source eBinders 
Relevancy:
75.55% 
 
Date/Time:
May 1, 2017   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Speaker:
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
17-3 - The Evolving Clinical Research Enterprise: What Recent Legal and Regulatory Changes Mean to You 
Relevancy:
82.76% 
 
Date/Time:
May 2, 2017   9:45am - 10:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
18-2 - Returning Research Test Results: Know Your Ethical and Legal Obligations 
Relevancy:
30.87% 
 
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 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
33.79% 
 
Date/Time:
April 16, 2016   9:00am - 10:30am
 
Total Credits:
1.5 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
2-2 - Advanced Monitoring Visit Documentation: Global Regulatory Authority Inspections and Sponsors 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
71.64% 
 
Date/Time:
April 16, 2016   2:30pm - 4:30pm
 
Total Credits:
2.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
2-8 - Clinical Trial Study Management Plans: The Architecture of a Quality Clinical Trial 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
30.52% 
 
Date/Time:
April 16, 2016   2:30pm - 4:30pm
 
Total Credits:
2.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
3-2 - Around the World in 120 Minutes: A Discussion of Global Research 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
48.74% 
 
Date/Time:
April 17, 2016   8:30am - 10:30am
 
Total Credits:
2.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
3-3 - I Think I Can: Ethical Considerations for the Cognitively Impaired 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
27.07% 
 
Date/Time:
April 17, 2016   8:30am - 10:30am
 
Total Credits:
2.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
3-5 - Regulatory and Ethical Considerations for Clinical Research Involving Mobile Technology 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
54.83% 
 
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 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
28.84% 
 
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 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
73.90% 
 
Date/Time:
April 17, 2016   10:45am - 11:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
4-8 - Before RBM was in Vogue: How NIH Managed Efficient Monitoring 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
59.81% 
 
Date/Time:
April 17, 2016   10:45am - 11:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
4-9 - CDER BIMO Compliance and Enforcement: What You Need to Know! 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
33.18% 
 
Date/Time:
April 17, 2016   10:45am - 11:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
5-3 - Dealing with Unanticipated Problems Involving Risk in Clinical Research 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
30.55% 
 
Date/Time:
April 17, 2016   4:15pm - 5:15pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
5-7 - Decoding the New Drug Good Clinical Practice Regulations 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
53.48% 
 
Date/Time:
April 17, 2016   4:15pm - 5:15pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
6-1 - Pregnancy Prevention During Trials: Beyond the Birds and the Bees 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
45.36% 
 
Date/Time:
April 18, 2016   8:30am - 10:00am
 
Total Credits:
1.5 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
7-7 - So, You Want to Be an Investigator: The Other Side of the Coin 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
37.59% 
 
Date/Time:
April 18, 2016   10:15am - 11:45am
 
Total Credits:
1.5 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
8-4 - EU Clinical Trials Regulation: Live in 2016? 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
30.60% 
 
Date/Time:
April 18, 2016   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
8-9 - Inside the FDA: Drug Good Clinical Practice Regulations Compliance 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
28.21% 
 
Date/Time:
April 18, 2016   2:30pm - 3:30pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
10-1 - Brain Tumors Under Attack: The "Shock and Awe" of Oncolytic Viruses 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
24.44% 
 
Date/Time:
April 19, 2016   9:45am - 10:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
10-6 - Special Considerations in Pediatric Trials for CRAs 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
50.14% 
 
Date/Time:
April 19, 2016   9:45am - 10:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
rating
10-8 - Standardizing Principal Investigator Delegation Records: An Alternative Approach for Sites 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
32.31% 
 
Date/Time:
April 19, 2016   9:45am - 10:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
10-9 - Interpreting Clinical Regulations: Precautions and Warnings 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
64.86% 
 
Date/Time:
April 19, 2016   9:45am - 10:45am
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
11-3 - The True Costs of Site Regulatory Compliance and Improvement Opportunities 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
93.43% 
 
Date/Time:
April 19, 2016   11:00am - 12:00pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
11-8 - Bench to Patient: The Device Regulatory Process 
$75.00
Purchase
Member Price:
$25.00
Relevancy:
85.07% 
 
Date/Time:
April 19, 2016   11:00am - 12:00pm
 
Total Credits:
1.0 CH  
 
Format:
       
  Synced Audio / Video / Slides
 

 
81 Results Found, Showing 1 - 50
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