Addendum to ICH S6 : preclinical safety evaluation of biotechnology-derived pharmaceuticals.

Other author United States. Food and Drug Administration.
Other author International Conference on Harmonisation.
Format Electronic
Publication Info[Rockville, Md.? : U.S. Dept. of Health and Human Services, Food and Drug Administration, 2009]
Description1 online resource (iv, 14 p.)
Supplemental Contenthttps://purl.fdlp.gov/GPO/LPS118023
Subjects

Portion of title Preclinical safety evaluation of biotechnology-derived pharmaceuticals
General note"ICH harmonised tripartite guideline."
General note"S6(R1)."
General note"Current step 2 version, dated October 29, 2009."
General noteGPO Cataloging Record Distribution Program (CRDP).
Bibliography noteIncludes bibliographical references (p. 14).
GPO item number0475 (online)
Govt. docs number HE 20.4002:B 52

Availability

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Electronic Resources Access Content Online ✔ Available