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Preparation of drug submissions : comparative bioavailability studies. (Therapeutic Products Directorate guidelines)

Preparation of drug submissions : comparative bioavailability studies. (Therapeutic Products Directorate guidelines)
Paper図書
Therapeutic Products Directorate, Health Canada1997.<Y629-98-170>
National Diet Library
  • Author HeadingCanada. Therapeutic Products Directorate.

General considerations for clinical trials : ICH harmonised tripartite guideline. (Therapeutic Products Directorate guidelines)

General considerations for clinical trials : ICH harmonised tripartite guideline. (Therapeutic Products Directorate guidelines)
Paper図書
Therapeutic Products Directorate, Health Canada[1997]<Y629-98-168>
National Diet Library
  • Author Heading...for Human Use. Canada. Therapeutic Products Directorate.

Timing of non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals : ICH harmonised tripartite guideline. (Therapeutic Products Directorate guidelines)

Timing of non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals : ICH harmonised tripartite guideline. (Therapeutic Products Directorate guidelines)
Paper図書
Therapeutic Products Directorate, Health Canada[1997]<Y629-98-169>
National Diet Library
  • Author Heading...for Human Use. Canada. Therapeutic Products Directorate.

Good clinical practice : consolidated guideline : ICH harmonised tripartite guideline. (Therapeutic Products Directorate guidelines)

Good clinical practice : consolidated guideline : ICH harmonised tripartite guideline. (Therapeutic Products Directorate guidelines)
Paper図書
Therapeutic Products Directorate[1997]<Y629-97-103>
National Diet Library
  • Author Heading...for Human Use. Canada. Therapeutic Products Directorate.

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