Identify the responsibilities of clinical trials sponsors and investigators. Recognize examples of Adverse Event Reporting (AER).Become familiar with the purposes of Bioresearch Monitoring (BIMO).
Christina Kuhn, Associate, Covington & Burling LLP
Amy Leiser, Associate, Covington & Burling LLP
This session was recorded as part of FDLI's Virtual Introduction to Medical Device Law and Regulation Course in April 2020.