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Addendum to ICH S6 preclinical safety evaluation of biotechnology-derived pharmaceuticals. Cover Image E-book

Addendum to ICH S6 [electronic resource] : preclinical safety evaluation of biotechnology-derived pharmaceuticals.

Preclinical safety evaluation of biotechnology-derived pharmaceuticals (portion title)
United States. Food and Drug Administration. (Added Author). International Conference on Harmonisation. (Added Author).

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Record details

  • Physical Description: 1 online resource (iv, 14 p.)
  • Publisher: [Rockville, Md.? : U.S. Dept. of Health and Human Services, Food and Drug Administration, 2009]

Content descriptions

General Note:
"Current step 2 version, dated October 29, 2009."
"ICH harmonised tripartite guideline."
"S6(R1)."
GPO Cataloging Record Distribution Program (CRDP).
Bibliography, etc. Note:
Includes bibliographical references (p. 14).

Search for related items by subject

Subject:
Drugs > Testing.
Pharmaceutical biotechnology.