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Disinfectant drugs. 1999 edition. (Therapeutic Products Programme guidelines)
Disinfectant drugs. 1999 edition. (Therapeutic Products Programme guidelines)
Paper
図書
Therapeutic Products Programme, Health Canada
1999.
<Y629-00-191>
National Diet Library
Impurities : guideline for residual solvents. CA1 NH24 99 I53 (Therapeutic Products Directorate guidelines)
Impurities : guideline for residual solvents. CA1 NH24 99 I53 (Therapeutic Products Directorate guidelines)
Paper
図書
Therapeutic Products Programme, Health Canada
1998.
<Y629-99-192>
National Diet Library
Impurities in new drug products. (Therapeutic Products Programme guideline)
Impurities in new drug products. (Therapeutic Products Programme guideline)
Paper
図書
Therapeutic Products Programme, Health Canada
1998.
<Y629-99-193>
National Diet Library
Stability testing : photostability testing of new drug substances and products. (Therapeutic Products Programme guideline)
Stability testing : photostability testing of new drug substances and products. (Therapeutic Products Programme guideline)
Paper
図書
Therapeutic Products Programme, Health Canada
1998.
<Y629-99-195>
National Diet Library
Validation of analytical procedures : methodology. CA1 NH24 98 V15 (Therapeutic Products Programme guideline)
Validation of analytical procedures : methodology. CA1 NH24 98 V15 (Therapeutic Products Programme guideline)
Paper
図書
Therapeutic Products Programme, Health Canada
[1998]
<Y629-99-197>
National Diet Library
Good manufacturing practices [5th edition].
Good manufacturing practices [5th edition].
Paper
図書
published by the authority of the Minister of Health.
Therapeutic Products Programme, Health Canada
[1998]
<Y629-99-191>
National Diet Library
Text on validation of analytical procedures. CA1 NH24 98 T25 (Therapeutic Products Programme guideline)
Text on validation of analytical procedures. CA1 NH24 98 T25 (Therapeutic Products Programme guideline)
Paper
図書
Therapeutic Products Programme, Health Canada
[1998]
<Y629-99-196>
National Diet Library
Conduct and analysis of bioavailability and bioequivalence studies. Part B Oral modified release formulations.
Conduct and analysis of bioavailability and bioequivalence studies. Part B Oral modified release formulations.
Paper
図書
Therapeutic Products Programme, Health Canada
[1996]
<Y629-97-102>
National Diet Library
Reached to the end of result.
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