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

Bibliographic Details
Corporate Authors:	Center for Drug Evaluation and Research (U.S.), 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:	Electronic filing systems > Government policy > United States. Drugs > Research > Government policy > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS113315

Description
Item Description:	Title from PDF title page (viewed on June 2, 2009). "June 2008". "Revision 2". Electronic resource.
Physical Description:	ii, 16 pages : digital, PDF file.
Format:	Mode of access: Internet at the FDA web site. Address as of 6/2/09: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM072349.pdf ; current access is available via PURL.