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

Description
Item Description:	Title from PDF title page (viewed on Apr. 23, 2009). "June 2008." "Revision 2." Electronic resource.
Physical Description:	ii, 16 pages : digital, PDF file.
Format:	Mode of access: Internet at the FDA CBER Web site. Address as of 4/23/09: http://www.fda.gov/cber/gdlns/esubapp.pdf ; current access is available via PURL.