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Preparing for FDA Pre-Approval Inspections
Seiten
1998
Marcel Dekker Inc (Verlag)
978-0-8247-0218-2 (ISBN)
Marcel Dekker Inc (Verlag)
978-0-8247-0218-2 (ISBN)
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Clarifies FDA requirements for the manufacture of clinical trial material, as well as product development activities, and suggests strategies that will facilitate FDA authorization to market.
This one-of-a-kind reference clarifies FDA requirements for the manufacture of clinical trial material as well as product development activities and suggests strategies that will facilitate FDA authorization to market.
This one-of-a-kind reference clarifies FDA requirements for the manufacture of clinical trial material as well as product development activities and suggests strategies that will facilitate FDA authorization to market.
Introduction to the Food and Drug Administration Pre-New Drug Applications Approval Inspections o Developing a Strategic Approach to Preparing for a Successful Pre-NDA Approval Inspection o Food and Drug Administration International Pre-Approval Inspections o Stability Data and Pre-Approval Inspections o Consequences of Failing a Pre-Approval Inspection o Successful Management of a Pre-Approval Inspection o The Validation of Pharmaceutical Processes o Documentation Standards for Pre-Approval Inspections o Technology Transfer and Scale-up o Training of Personnel in the Pharmaceutical Industry o Compliance with Current Good Manufacturing Practices and Application Commitments
Erscheint lt. Verlag | 15.10.1998 |
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Reihe/Serie | Drugs and the Pharmaceutical Sciences |
Verlagsort | New York |
Sprache | englisch |
Maße | 152 x 229 mm |
Gewicht | 454 g |
Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete ► Pharmakologie / Pharmakotherapie |
Technik | |
ISBN-10 | 0-8247-0218-2 / 0824702182 |
ISBN-13 | 978-0-8247-0218-2 / 9780824702182 |
Zustand | Neuware |
Informationen gemäß Produktsicherheitsverordnung (GPSR) | |
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109,00 €