ICH harmonized tripartite guideline: Timing of non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals : International Conference on Harmonization of Technical Requirements...: H42-2/67-13-1997E
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| Department/Agency | Canada. Health Canada. Therapeutic Products Directorate. |
|---|---|
| Title | ICH harmonized tripartite guideline: Timing of non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals : International Conference on Harmonization of Technical Requirements for the Registration of Pharmaceuticals for Human Use |
| Series title | Therapeutic Products Directorate guidelines |
| Publication type | Series - View Master Record |
| Language | [English] |
| Format | Paper |
| Other formats | Electronic-[English] |
| Publishing information | Ottawa - Ontario : Health Canada. 1997. |
| Binding | Loose-leaf |
| Description | 9p. ; 28 cm. |
| ISBN | 0-662-26386-3 |
| Catalogue number |
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