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The End of an Era: FDA Announces Disposition Plans for COVID-19 Related Guidance Documents | Wiley Rein LLP
The COVID-19 pandemic presented the U.S. Food and Drug Administration (FDA or Agency) with a monumental task of shifting its operations and the way it approached the regulation of.
Health care professionals
Public health emergency on formal meetings
Drug administration
Development of abbreviated new drug applications during
Public health emergency
Public health emergency revised
Health emergency
Federal register
Guidance documents that will expire with
Transition plan
Investigational cellular
Gene therapy products during
Abbreviated new drug applications during
Formal meetings
User fee applications questions
Certain drugs
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