Regulatory scripting: Stakeholder participation in food and drug administration medical device advisory meetings

In an age of biomedicalization, medical devices have become more common and more technologically complicated, and adverse events associated with medical devices have increased. The U.S. Food and Drug Administration (FDA) relies on advisory panels to assist in regulatory decision making regarding med...

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Bibliographic Details
Main Authors: Shelley K. White, Valerie Leiter, Mi H. Le, Caitlyn K. Helms
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934387/?tool=EBI