Timing of non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals : ICH harmonized tripartite guideline, International Conference on Harmonisation of Technical Requirements...: H42-2/67-13-1997E-PDF

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Publication information
Department/Agency Canada. Health Canada. Therapeutic Products Directorate.
Title Timing of non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals : ICH harmonized tripartite guideline, International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / Published by authority of the Minister of Health.
Series title Therapeutic Products Directorate guidelines
Publication type Series - View Master Record
Language [English]
Other language editions [French]
Format Electronic
Electronic document
Other formats Paper-[English]
Note(s) Incorrect catalogue number (H42-2/67-13-1997IN) and ISBN (0-662-26386-3) copied in this electronic publication.
Includes some text in French.
Publishing information Ottawa - Ontario : Health Canada. June 18, 1998, c1997.
Description 19p.references, tables
Catalogue number
  • H42-2/67-13-1997E-PDF
Subject terms Pharmacology
Toxicology
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