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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Detalles Bibliográficos
Autores principales: White, Shelley K., Leiter, Valerie, Le, Mi H., Helms, Caitlyn K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934387/
https://www.ncbi.nlm.nih.gov/pubmed/36795788
http://dx.doi.org/10.1371/journal.pone.0281774

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934387/
https://www.ncbi.nlm.nih.gov/pubmed/36795788
http://dx.doi.org/10.1371/journal.pone.0281774

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