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IND-Enabling Non-Clinical Safety Assessment of Candidate Drugs and Good Laboratory Practice Standards: The FDA Regulatory Perspective

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Air date: Monday, September 29, 2014, 2:00:00 PM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 322 (157 Live, 165 On-demand)
Category: Special
Runtime: 01:42:07
Description: IND-Enabling Non-Clinical Safety Assessment of Candidate Drugs and Good Laboratory Practice Standards: The FDA Regulatory Perspective

An educational program of the NIH Clinical Center-FDA CDER Joint Task Force
NLM Title: IND-enabling non-clinical safety assessment of candidate drugs and good laboratory practice standards : the FDA regulatory perspective / Juan Lertora.
Author: Lertora, Juan.
National Institutes of Health (U.S.),
Publisher:
Abstract: (CIT): IND-Enabling Non-Clinical Safety Assessment of Candidate Drugs and Good Laboratory Practice Standards: The FDA Regulatory Perspective An educational program of the NIH Clinical Center-FDA CDER Joint Task Force.
Subjects: Clinical Trials as Topic--standards
Drug Approval--statistics & numerical data
Drug Evaluation--standards
Federal Government
Government Agencies
United States
Publication Types: Lecture
Webcast
NLM Classification: QV 771.4
NLM ID: 101645865
CIT Live ID: 14681
Permanent link: https://videocast.nih.gov/watch=14681

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