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Record 5 of 5
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Title
Guidance for industry [electronic resource] : Q3B(R2) impurities in new drug products.
Imprint
Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2006]
Connect to
Connect to https://permanent.fdlp.gov/LPS113762/LPS113762/www.fda.gov/downloads/RegulatoryInformation/Guidances/ucm128033.pdf
Copies
Location
Call No.
OPAC Message
Status
Axe Federal Documents Online
HE 20.4702:IM 7/2
---
Available
Description
8 p. : digital, PDF file
System Details
Mode of access via the FDA web site.
Note
Title from PDF title page (viewed on June 15, 2009).
"ICH".
"July 2006" .
"Revision 2".
Subject
Drug development -- Government policy -- United States.
Drug adulteration -- Government policy -- United States.
Added Author
Center for Drug Evaluation and Research (U.S.)
Center for Biologics Evaluation and Research (U.S.)
International Conference on Harmonisation.
Added Title
Q3B(R2) impurities in new drug products
Impurities in new drug products
Gpo Item No.
0499-T (online)
Sudoc No.
HE 20.4702:IM 7/2
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