Summary:

The Clinical Trials Registration and Results Reporting course is for investigators responsible for clinical trials.gov registration and results reporting for applicable clinical trials. The course will help investigators understand the Federal and Institutional requirements for clinical trials registration and results reporting. This is a great course to include as a part of onboarding, and it is also a great refresher for experienced Investigators to ensure they are aware of the most current regulations, institutional policies, and best practices for clinicaltrials.gov compliance.

Sample of Topics:

• Rules
• Registration
• Record Review Process
• Record Maintenance
• Noncompliance
• Resources

Speakers:

• Pamela Richtmyer – Director, MGB Human Research Affairs Compliance & Education Office
• Kathy Vernovsky – MGB Human Research Affairs Compliance & Education Office

Additional Details:

• The ClinicalTrials.gov training will be offered monthly through the MGB Human Research Affairs Compliance & Education Office. Future dates can be found here.
• RCR Eligibility: Completion of this session fulfills 1 of the 4 hours outlined in part 3 of the RCR requirement.

**This session will be held virtually. The link will be sent to those who register with a BWH/MGB-affiliated email address ~1 day prior to the session**

CLICK HERE TO REGISTER