Analytical Chemistry in a GMP Environment
A Practical Guide
2007
John Wiley & Sons Inc (Hersteller)
978-0-471-23176-9 (ISBN)
John Wiley & Sons Inc (Hersteller)
978-0-471-23176-9 (ISBN)
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Provides guidance for laboratory analysts who juggle the Food and Drug Administration's good manufacturing practice (GMP) rules with changing analytical technologies. A manual for formal training as well a self-study guide, this book includes instructions on various analytical chemical methods, from spectroscopy to chromatography to dissolution.
How to hone your analytical skills and obtain high-quality data in the era of GMP requirements? With increased regulatory pressures on the pharmaceutical industry, there is a growing need for capable analysts who can ensure appropriate scientific practices in laboratories and manufacturing sites worldwide. Based on Johnson & Johnson's acclaimed in-house training program, this practical guide provides guidance for laboratory analysts who must juggle the Food and Drug Administration's good manufacturing practices (GMP) rules with rapidly changing analytical technologies. Highly qualified industry experts walk readers step-by-step through the concepts, techniques, and tools necessary to perform analyses in an FDA-regulated environment, including clear instructions on all major analytical chemical methods - from spectroscopy to chromatography to dissolution.
An ideal manual for formal training as well as an excellent self-study guide, "Analytical Chemistry in a GMP Environment" features: the drug development process in the pharmaceutical industry; uniform and consistent interpretation of GMP compliance issues; a review of the role of statistics and basic topics in analytical chemistry, and an emphasis on high-performance liquid chromatographic (HPLC) methods; chapters on detectors and quantitative analysis as well as data systems; methods for ensuring that instruments meet standard operating procedures (SOP) requirements; and extensive appendixes for unifying terms, symbols, and procedural information.
How to hone your analytical skills and obtain high-quality data in the era of GMP requirements? With increased regulatory pressures on the pharmaceutical industry, there is a growing need for capable analysts who can ensure appropriate scientific practices in laboratories and manufacturing sites worldwide. Based on Johnson & Johnson's acclaimed in-house training program, this practical guide provides guidance for laboratory analysts who must juggle the Food and Drug Administration's good manufacturing practices (GMP) rules with rapidly changing analytical technologies. Highly qualified industry experts walk readers step-by-step through the concepts, techniques, and tools necessary to perform analyses in an FDA-regulated environment, including clear instructions on all major analytical chemical methods - from spectroscopy to chromatography to dissolution.
An ideal manual for formal training as well as an excellent self-study guide, "Analytical Chemistry in a GMP Environment" features: the drug development process in the pharmaceutical industry; uniform and consistent interpretation of GMP compliance issues; a review of the role of statistics and basic topics in analytical chemistry, and an emphasis on high-performance liquid chromatographic (HPLC) methods; chapters on detectors and quantitative analysis as well as data systems; methods for ensuring that instruments meet standard operating procedures (SOP) requirements; and extensive appendixes for unifying terms, symbols, and procedural information.
| Erscheint lt. Verlag | 17.9.2007 |
|---|---|
| Verlagsort | New York |
| Sprache | englisch |
| Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete ► Pharmakologie / Pharmakotherapie |
| Technik | |
| Wirtschaft ► Betriebswirtschaft / Management ► Unternehmensführung / Management | |
| ISBN-10 | 0-471-23176-2 / 0471231762 |
| ISBN-13 | 978-0-471-23176-9 / 9780471231769 |
| Zustand | Neuware |
| Informationen gemäß Produktsicherheitsverordnung (GPSR) | |
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