Guidance for industry : E2E pharmacovigilance planning.

Bibliographic Details
Corporate Authors:	Center for Drug Evaluation and Research (U.S.), Center for Biologics Evaluation and Research (U.S.), International Conference on Harmonisation
Format:	Government Document Conference Proceeding eBook
Language:	English
Published:	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, [2005]
Subjects:	Drug development. Drugs > Side effects.
Online Access:	https://purl.fdlp.gov/GPO/LPS113917

Description
Item Description:	Title from PDF title page (viewed on June 19, 2009). "ICH". "April 2005". Electronic resource.
Physical Description:	18 pages : digital, PDF file.
Format:	Mode of access: Internet at the FDA web site. Address as of 6/19/09: http://www.fda.gov/downloads/RegulatoryInformation/Guidances/ucm129423.pdf ; current access is available via PURL.
Bibliography:	Includes bibliographical references (pages 17-18).