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  • 1
    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.
    Library Location Call Number Volume/Issue/Year Availability
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