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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

Permanent link to this Catalogue record:
publications.gc.ca/pub?id=9.573944&sl=0

Publication information
Department/Agency
  • Canada. Health Canada. Therapeutic Products Directorate.
TitleTiming 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 typeMonograph - View Master Record
Language[English]
Other language editions[French]
FormatDigital text
Electronic document
Other formatsPhysical text-[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.
Description19p.references, tables
Catalogue number
  • H42-2/67-13-1997E-PDF
Subject terms
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