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Legal Aspects of FDA approval and implications for clinical research

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Manage episode 326134154 series 3325094
Content provided by Thomas Nero MD FACC. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Thomas Nero MD FACC or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.

We would love to hear your thoughts on the episodes!

Prof. Christine Coughlin of Wake Forest School of Law speaks with Dr. Thomas Nero on the FDA approval process, emergency use authorization, Right to Try Legislation and the implications for clinical research, diversity and health care equity. Prof. Coughlin holds positions in the College of Medicine as well as the Law school and in the Center for Bioethics. She has published extensively on the FDA approval process.

  continue reading

22 episodes

Artwork
iconShare
 
Manage episode 326134154 series 3325094
Content provided by Thomas Nero MD FACC. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Thomas Nero MD FACC or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.

We would love to hear your thoughts on the episodes!

Prof. Christine Coughlin of Wake Forest School of Law speaks with Dr. Thomas Nero on the FDA approval process, emergency use authorization, Right to Try Legislation and the implications for clinical research, diversity and health care equity. Prof. Coughlin holds positions in the College of Medicine as well as the Law school and in the Center for Bioethics. She has published extensively on the FDA approval process.

  continue reading

22 episodes

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