Guidance for industry : providing regulatory submissions in electronic format : human pharmaceutical product applications and related submissions using the eCTD specifications.

Bibliographic Details
Corporate Author:	Center for Biologics Evaluation and Research (U.S.)
Format:	Government Document eBook
Language:	English
Published:	Silver Spring, MD : 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, [2008]
Subjects:	Center for Drug Evaluation and Research (U.S.) Drug approval > United States. Electronic filing systems > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS111798