UID:
almahu_9949385907802882
Format:
1 online resource
Edition:
Third edition.
ISBN:
9781315102948
,
1315102943
,
9781351593595
,
1351593595
,
9781351593601
,
1351593609
,
9781351593588
,
1351593587
Note:
Previous edition: New York: Informa Healthcare, 2009.
,
Part I. Regulatory and Manufacturing Guidelines; Chapter 1. U.S. FDA Good Manufacturing Practices; Chapter 2. Guideline on the Common Technical Document for the Registration of Pharmaceuticals for Human Use; Chapter 3. Process Validation: General Principles and Practices; Chapter 4. Bioequivalence Regulatory Compliance; Chapter 5. Bioequivalence Regulatory Review Process and Audit; Chapter 6. EU Guidelines to Good Manufacturing Practice: Active Drug Substance; Chapter 7. FDA Pre-approval Inspections; Chapter 8. Formulation Factors in Uncompressed Dosage Forms; Chapter 9: Solid-State Properties.; Chapter 10: Formulation of Flavor.; Part II. Manufacturing Formulations; Uncompressed Solids Formulations; Part III. Commercial Pharmaceutical Formulations.; Commercial Pharmaceutical Formulations.
Additional Edition:
Print version : ISBN 9781138103160
Language:
English
Keywords:
Electronic books.
;
Electronic books.
DOI:
10.1201/9781315102948
URL:
https://www.taylorfrancis.com/books/9781315102948
