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| 01063nam##2200241za#4500 |
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| 001 | 9.614225 |
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| 003 | CaOODSP |
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| 005 | 20200327132858 |
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| 007 | ta |
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| 008 | 150406|1997||||xxc||||| f|0| 0 eng|d |
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| 020 | |a0-662-26386-3 |
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| 040 | |aCaOODSP|beng |
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| 043 | |an-cn--- |
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| 086 | 1 |aH42-2/67-13-1997E |
|---|
| 110 | 1 |aCanada.|bHealth Canada. |bTherapeutic Products Directorate. |
|---|
| 245 | 10|aICH harmonized tripartite guideline: Timing of non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals : |bInternational Conference on Harmonization of Technical Requirements for the Registration of Pharmaceuticals for Human Use |
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| 260 | |aOttawa - Ontario : |bHealth Canada. |c1997. |
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| 300 | |a9p. ; |c28 cm. |
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| 490 | 1 |aTherapeutic Products Directorate guidelines |
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| 563 | |aLoose-leaf |
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| 590 | |a98-38|b1998-09-18 |
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| 776 | 0#|tTiming of non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals : |w(CaOODSP)9.573944 |
|---|
| 830 | #0|aTherapeutic Products Directorate guidelines.|w(CaOODSP)9.514729 |
|---|