U.S. flag An official website of the United States government
  1. Home
  2. Drugs
  3. News & Events for Human Drugs
  4. CDER BIMO GCP Compliance and Enforcement - 02/16/2022
  1. News & Events for Human Drugs


Event Title
CDER BIMO GCP Compliance and Enforcement
February 16, 2022

February 16, 2022
1:00 PM - 3:30 PM ET


Visit CDER Small Business and Industry Assistance Page


This webinar will:

  • Provide a general overview of the Bioresearch Monitoring (BIMO) program
  • Discuss Good Clinical Practice (GCP) inspectional processes, compliance evaluation and enforcement, including case examples 
  • Summarize findings from a recent publication on follow-up inspectional activities after FDA notifies an inspected entity of serious-noncompliance
  • Include live Q&A session and a moderated panel discussion


  • Overview of CDER’s GCP BIMO Program
  • GCP inspections, including classification criteria, and case examples of serious non-compliance
  • Official Action Indicated (OAI) follow-up inspection procedures, findings, and trends


  • Clinical investigators
  • Clinical research personnel (e.g., sub-investigators, study coordinators, regulatory specialists)
  • Sponsors, Contract Research Organizations (CROs)
  • Sponsor-Investigators
  • Institutional Review Board (IRBs)



Real-time attendance is required for the certificate of attendance which can be used in support of CEs for the following professional organizations. Certificates are only available during the two weeks post-event.

This course has been:

  • pre-approved by RAPS as eligible for a maximum of 12 credits for a two day event (appropriate to real-time attendance) towards a participant’s RAC recertification upon full completion.
  • pre-approved by SOCRA who accepts documentation of candidate participation in continuing education programs for re-certification if the program is applicable to clinical research regulations, operations or management, or to the candidate's clinical research therapeutic area.
  • pre-approved by SQA as eligible for 1 non-GCP or non-GLP unit for every 1 hour of instructional time towards a participant’s RQAP re-registration.
  • approved by ACRP for continuing education in clinical research. ACRP will provide 1 ACRP contact hour for every 45-60 minutes of qualified material.


  • To optimize your webinar experience, use Chrome when viewing AdobeConnect in a browser.
  • Please contact [email protected] for all technical questions.
  • If you encounter any technical issues before or during the event, please visit the Technical Issues Support
  • Test your PC for use with Adobe Connect prior to the day of the event. Adobe, the Adobe logo, Acrobat and Acrobat Connect are either registered trademarks or trademarks of Adobe Systems Incorporated in the United States and/or other countries.
Back to Top