Pamela Richtmyer - Director, MGB Human Research Affairs Compliance & Education
Kathy Vernovsky - MGB Human Research Affairs Compliance & Education
This session is offered to investigators and study staff to provide the tools to navigate the ClinicalTrials.gov database proficiently and ensure compliance with current regulatory requirements.
The workshop will include a practical summary of current regulatory requirements and consequences of noncompliance, technical training to complete the registration and results reporting modules, and tips and considerations to avoid common errors. A live walk through a test record in the database will be included.
Target Audience: Investigators and study staff who are conducting clinical trials and need to register on ClinicalTrials.gov.