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Title
Addendum to ICH S6 [electronic resource] : preclinical safety evaluation of biotechnology-derived pharmaceuticals.
Imprint
[Rockville, Md.? : U.S. Dept. of Health and Human Services, Food and Drug Administration, 2009]
Connect to
Connect to https://permanent.fdlp.gov/websites/www.fda.gov/pdf-archive/UCM194490.pdf
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Axe Federal Documents Online
HE 20.4002:B 52
---
Available
Description
1 online resource (iv, 14 p.)
Note
"ICH harmonised tripartite guideline."
"S6(R1)."
"Current step 2 version, dated October 29, 2009."
Bibliography
Includes bibliographical references (p. 14).
Subject
Pharmaceutical biotechnology.
Drugs -- Testing.
Added Author
United States. Food and Drug Administration.
International Conference on Harmonisation.
Added Title
Preclinical safety evaluation of biotechnology-derived pharmaceuticals
Gpo Item No.
0475 (online)
Sudoc No.
HE 20.4002:B 52
Available items only
