Guidance for industry : providing regulatory submissions in electronic format, general considerations.

Guidance for industry : providing regulatory submissions in electronic format, general considerations.

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Bibliographic Details
Imprint:Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [1999]
Description:1 online resource (17 pages)
Language:English
Subject:
Electronic filing systems -- Government policy -- United States.
Drug approval -- United States.
Format: E-Resource U.S. Federal Government Document Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/7894427
Hidden Bibliographic Details
Varying Form of Title:Providing regulatory submissions in electronic format, general considerations
Other authors / contributors:Center for Drug Evaluation and Research (U.S.)
Center for Biologics Evaluation and Research (U.S.)
Notes:"IT 2."
"January 1999."
GPO item no.:0499-T (online)
Govt.docs classification:HE 20.4702:R 26/8 HE 20.4702:R 26

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