Guidance for industry : 21 CFR part 11, electronic records, electronic signatures, validation.

Bibliographic Details
Corporate Authors:	United States. Food and Drug Administration. Office of Regulatory Affairs, Center for Biologics Evaluation and Research (U.S.), Center for Drug Evaluation and Research (U.S.), Center for Devices and Radiological Health (U.S.), Center for Food Safety and Applied Nutrition (U.S.), Center for Veterinary Medicine (U.S.)
Format:	Government Document eBook
Language:	English
Published:	Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of Regulatory Affairs : Center for Biologics Evaluation and Research : Center for Drug Evaluation and Research : Center for Devices and Radiological Health : Center for Food Safety and Applied Nutrition : Center for Veterinary Medicine, [2001]
Subjects:	Electronic records > Government policy > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS115328

Description
Item Description:	Title from PDF title page (viewed on July 27, 2009). "Draft guidance". "August 2001". Electronic resource.
Physical Description:	iii, 21 pages : digital, PDF file.
Format:	Mode of access: Internet at the FDA web site. Address as of 7/27/09: http://www.fda.gov/downloads/RegulatoryInformation/Guidances/UCM124946.pdf ; current access is available via PURL.
Bibliography:	Includes bibliographical references (pages 15-21).