Medical Device Clinical Investigations: An Introduction to Sponsor Responsibilities and Compliance Issues

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).

Rebecca Jones McKnight, Partner, DLA Piper LLP (US)

This session was recorded as part of FDLI’s Virtual Introduction to Medical Device Law and Regulation Course in November 2022. 

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