Building a ClinicalTrials.gov Compliance Program – Tips for Investigators and Institutions

Review reporting regulations, learn about noncompliance, and discuss how to build a successful compliance monitoring program.

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About this Webinar


This webinar covers a brief overview of the regulations, important timelines to follow, agency-specific variances, and a range of compliance mechanisms. It also covers the specific steps a major university took to build a successful compliance program to assist investigators. It concludes with information on how to connect with a national taskforce, which provides resources that help organizations become more compliant.

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Language Availability: English

Suggested Audiences: Clinical Researchers, Clinical Research Coordinators, Investigators, Sponsors

Organizational Subscription Price: $300 per year/per site or included as part of the $1,000 annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person


Webinar Content


Building a ClinicalTrials.gov Compliance Program – Tips for Investigators and Institutions

Presented by: Anthony Keyes, MBA, PMP - Johns Hopkins University

This webinar reviews the main regulations and policies that govern clinical trial registration and results reporting. It also describes the risks and liabilities involved with noncompliance and discusses how organizations can build compliance monitoring programs.

Recommended Use: Required
ID (Language): 19747 (English)