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Guidance for industry : Q3A impurities in new drug substances.

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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, [2008]
Subjects:
Drug development > Government policy > United States.
Drug adulteration > Government policy > United States.
Online Access:https://purl.fdlp.gov/GPO/LPS113736
Description
Item Description:Title from PDF title page (viewed on June 15, 2009).
"ICH".
"June 2008".
"Revision 2".
Electronic resource.
Physical Description:14 pages : digital, PDF file.
Format:Mode of access: Internet at the FDA web site. Address as of 6/15/09: http://www.fda.gov/downloads/RegulatoryInformation/Guidances/ucm127984.pdf ; current access is available via PURL.