Course Description

As the clinical research environment evolves in response to both internal and external changes, regulatory agency communication appears to be focused on particular areas of GCP compliance. Regulatory agencies’ recent findings for Clinical Investigators, sponsors, and Institutional Review Boards (IRBs) tend to reflect historic areas of noncompliance; however, more attention is being placed on ensuring that corrective and preventive action plans are developed to secure compliance. This web seminar will examine the trends in recent regulatory communication and open discussion for review of acceptable versus unacceptable responses.

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Learning Objectives

• Review recent FDA, European Medicines Agency (EMA), and Health Canada findings for Clinical Investigators (sites), sponsors, and IRBs
• Determine areas of compliance concentration for regulatory agencies
• Discuss what factors may be helping drive the present approach and what it may mean for future compliance considerations
• Examine best practices for responding to a regulatory communication

Who Should Attend

• Clinical Research Associates
• Project Managers
• Principal Investigators
• Clinical Research Coordinators
• IRB Administrators and Members
• Clinical Quality Assurance Auditors
• All other personnel responsible for ensuring compliance with GCP regulations

Instructor

Elizabeth Ronk Nelson, M.P.H.

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Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.