Handbook of Pharmaceutical Manufacturing Formulations
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Published By CRC Press

9781420081268, 9781420081275

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Front Matter

Handbook of Pharmaceutical Manufacturing Formulations ◽

10.3109/9781420081275-1 ◽

2009 ◽

pp. i-xxi

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Pharmaceutical Quality System

Handbook of Pharmaceutical Manufacturing Formulations ◽

10.3109/9781420081275-5 ◽

2009 ◽

pp. 24-31

Keyword(s):

Quality System ◽

Pharmaceutical Quality ◽

Pharmaceutical Quality System

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Index

Handbook of Pharmaceutical Manufacturing Formulations ◽

10.3109/9781420081275-25 ◽

2009 ◽

pp. 335-345

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GMP Audit Template, EU Guidelines (http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol4 en.htm)

Handbook of Pharmaceutical Manufacturing Formulations ◽

10.3109/9781420081275-20 ◽

2009 ◽

pp. 136-157

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Impurities in New Drug Products

Handbook of Pharmaceutical Manufacturing Formulations ◽

10.3109/9781420081275-18 ◽

2009 ◽

pp. 123-129

Keyword(s):

Drug Products ◽

New Drug

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Good Manufacturing Requirements for Active Pharmaceutical Ingredients

Handbook of Pharmaceutical Manufacturing Formulations ◽

10.3109/9781420081275-13 ◽

2009 ◽

pp. 79-80

Keyword(s):

Active Pharmaceutical Ingredients ◽

Pharmaceutical Ingredients

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Pharmaceutical Development

Handbook of Pharmaceutical Manufacturing Formulations ◽

10.3109/9781420081275-6 ◽

2009 ◽

pp. 32-38

Keyword(s):

Pharmaceutical Development

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FDA Active Pharmaceutical Ingredient Manufacturing Facility Inspection

Handbook of Pharmaceutical Manufacturing Formulations ◽

10.3109/9781420081275-14 ◽

2009 ◽

pp. 81-93 ◽

Cited By ~ 1

Keyword(s):

Active Pharmaceutical Ingredient ◽

Manufacturing Facility

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Validation of Analytical Procedures

Handbook of Pharmaceutical Manufacturing Formulations ◽

10.3109/9781420081275-11 ◽

2009 ◽

pp. 70-73

Keyword(s):

Analytical Procedures

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Manufacturing Formulations

Handbook of Pharmaceutical Manufacturing Formulations ◽

10.3109/9781420081275-23 ◽

2009 ◽

pp. 182-182

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Handbook of Pharmaceutical Manufacturing FormulationsLatest Publications

TOTAL DOCUMENTS

H-INDEX

Published By CRC Press

Front Matter

Pharmaceutical Quality System

Index

GMP Audit Template, EU Guidelines (http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol4 en.htm)

Impurities in New Drug Products

Good Manufacturing Requirements for Active Pharmaceutical Ingredients

Pharmaceutical Development

FDA Active Pharmaceutical Ingredient Manufacturing Facility Inspection

Validation of Analytical Procedures

Manufacturing Formulations

Handbook of Pharmaceutical Manufacturing Formulations
Latest Publications