International Conference on Harmonisation; Guidance on Nonclinical Safety Studies for the Conduct of Human Clinical Trials for Pharmaceuticals
Federal Register 1997 November 25; 62(227): 62922-62925 [Online] Available: http://frwebgate.access.gpo.gov.cgi-bin/multidb.cgi [23 February 2004]
Permanent LinkFind in a Library
Showing items related by title, author, creator and subject.
Guidance for Industry: M3(r2) Nonclinical Safety Studies for the Conduct of Human Clinical Trials and Marketing Authorization for Pharmaceuticals Unknown creator (United States. Department of Health and Human Services; United States. Food and Drug Administration; Center for Biologics Evaluation and Research (U.S.); and Center for Drug Evaluation and Research (U.S.), 2010)
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) Adopts Consolidated Guideline on Good Clinical Practice in the Conduct of Clinical Practice in the Conduct of Clinical Trials on Medicinal Products for Human Use Unknown creator (1997)