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| 01709nam##2200289za#4500 |
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| 001 | 9.573944 |
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| 003 | CaOODSP |
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| 005 | 20210624183938 |
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| 007 | cr ||||||||||| |
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| 008 | 150406|1997||||xxc|||||o f|0| 0 eng|d |
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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-PDF |
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| 110 | 1 |aCanada.|bHealth Canada. |bTherapeutic Products Directorate. |
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| 245 | 10|aTiming of non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals : |h[electronic resource]|bICH harmonized tripartite guideline, International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / |cPublished by authority of the Minister of Health. |
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| 260 | |aOttawa - Ontario : |bHealth Canada. |cJune 18, 1998, c1997. |
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| 300 | |a19p.|breferences, tables |
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| 490 | 1 |aTherapeutic Products Directorate guidelines |
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| 500 | |aIncorrect catalogue number (H42-2/67-13-1997IN) and ISBN (0-662-26386-3) copied in this electronic publication. |
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| 546 | |aIncludes some text in French. |
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| 590 | |a12-21-Supp|b2012-05-18 |
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| 690 | 07|aPharmacology|2gcpds |
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| 690 | 07|aToxicology|2gcpds |
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| 775 | 08|tCalendrier des études d'innocuité non cliniques pour la conduite d'essais cliniques de produits pharmaceutiques sur les sujets humains : |w(CaOODSP)9.603919 |
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| 776 | 0#|tICH harmonized tripartite guideline: Timing of non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals : |w(CaOODSP)9.614225 |
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| 830 | #0|aTherapeutic Products Directorate guidelines.|w(CaOODSP)9.506920 |
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| 856 | 40|ahttp://publications.gc.ca|qPDF|s42 KB|uhttps://publications.gc.ca/collections/Collection/H42-2-67-13-1997E.pdf |
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