Guidance for industry : S1B testing for carcinogenicity of pharmaceuticals.

Other author Center for Drug Evaluation and Research (U.S.)
Other author Center for Biologics Evaluation and Research (U.S.)
Other author International Conference on Harmonisation.
Format Electronic
Publication InfoRockville, 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, [1997]
Description10 p. : digital, PDF file
Supplemental Contenthttps://purl.fdlp.gov/GPO/LPS113890
Subjects

Portion of title S1B testing for carcinogenicity of pharmaceuticals
Portion of title Testing for carcinogenicity of pharmaceuticals
General noteTitle from PDF title page (viewed on June 18, 2009).
General note"ICH".
General note"July 1997".
General noteGPO Cataloging Record Distribution Program (CRDP).
Bibliography noteIncludes bibliographical references (p. 10).
Technical detailsMode of access: Internet at the FDA web site. Address as of 6/18/09: http://www.fda.gov/downloads/RegulatoryInformation/Guidances/UCM129221.pdf ; current access is available via PURL.
GPO item number0499-T (online)
Govt. docs number HE 20.4702:C 17

Availability

Library Location Call Number Status Item Actions
Electronic Resources Access Content Online ✔ Available