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Investigational New Drug (IND) Submission: Content/Format and First 30 Days (5of14) REdI 2018

REdI

CDER

FDA

SBIA

Автор: U.S. Food and Drug Administration

Загружено: 15 мая 2020 г.

Просмотров: 13 471 просмотр

Описание:

CDER’s Maureen Dillon-Parker and Judit Milstein discuss the content and format of an initial IND submission and what to expect during the first 30 days, including processes for clinical holds and best practices.
_______________________________
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Email: [email protected]
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Investigational New Drug (IND) Submission: Content/Format and First 30 Days (5of14) REdI 2018

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