Pharmaceutical manufacturing handbook regulations and quality
With its coverage of Food and Drug Administration regulations, international regulations, good manufacturing practices, and process analytical technology, this handbook offers complete coverage of the regulations and quality control issues that govern pharmaceutical manufacturing. In addition, the b...
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| Hlavní autor: | |
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| Médium: | E-kniha Kniha |
| Jazyk: | angličtina |
| Vydáno: |
Hoboken, N.J
Wiley-Interscience
2008
John Wiley & Sons, Incorporated Wiley-Blackwell |
| Vydání: | 1st ed. |
| Edice: | Pharmaceutical development series |
| Témata: | |
| ISBN: | 9780470259825, 9780470259597, 0470259590, 0470259825, 0470259833, 9780470259832 |
| On-line přístup: | Získat plný text |
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| Shrnutí: | With its coverage of Food and Drug Administration regulations, international regulations, good manufacturing practices, and process analytical technology, this handbook offers complete coverage of the regulations and quality control issues that govern pharmaceutical manufacturing. In addition, the book discusses quality assurance and validation, drug stability, and contamination control, all key aspects of pharmaceutical manufacturing that are heavily influenced by regulatory guidelines. The team of expert authors offer you advice based on their own firsthand experience in all phases of pharmaceutical manufacturing. |
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| Bibliografie: | Includes bibliographical references and index |
| ISBN: | 9780470259825 9780470259597 0470259590 0470259825 0470259833 9780470259832 |
| DOI: | 10.1002/9780470259832 |

