Clinical Investigations, Investigational Device Exemption (IDE), Institutional Review Boards (IRBs), and Informed Consent

Blake Wilson spoke on Clinical Investigations: Investigational Device Exemption (IDE), Institutional Review Boards (IRBs), and informed Consent at the Food and Drug Law Institute's Introduction to Medical Device Law and Regulation in Washington, D.C.

The event was held as a part of the Continuing Legal Education program and gave attendees an understanding of administrative agencies' effect on the medical industry. Blake also spoke on Premarket Approval Application (PMA); Humanitarian Device Exemption (HDE).

Learn More: Introduction to Medical Device Law and Regulation


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