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).
This session was recorded as part of FDLI’s Virtual Introduction to Medical Device Law and Regulation Course in April 2020.
- +$100 for nonmembers
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CLE credit is not currently available for pre-recorded sessions.