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Pharmaceutical Quality Systems

Medium: Buch
ISBN: 978-0-367-39870-5
Verlag: CRC Press
Erscheinungstermin: 19.09.2019
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When a pharmaceutical company decides to build a Quality System, it has to face the fact that there aren't any guideline that define exactly how such a system has to be built. With terms such as quality system, quality assurance, and quality management used interchangeably, even defining the system's objectives is a problem. This book provides a practical guide to building a quality system. Beginning with explanations of key terms and concepts, it covers ISO 9000 and GMP and how to combine them, and includes a matrix showing their similarities and differences. Implementation reviews illustrate how Quality (Management) Systems have been installed successfully in pharmaceutical companies. Also covered are the individual components of a Quality System; auditing, validation, and supplier qualification systems; and Hazard Analysis Critical Control Points (HACCP).


Produkteigenschaften


  • Artikelnummer: 9780367398705
  • Medium: Buch
  • ISBN: 978-0-367-39870-5
  • Verlag: CRC Press
  • Erscheinungstermin: 19.09.2019
  • Sprache(n): Englisch
  • Auflage: 1. Auflage 2019
  • Produktform: Kartoniert, Paperback
  • Gewicht: 569 g
  • Seiten: 392
  • Format (B x H x T): 152 x 229 x 21 mm
  • Ausgabetyp: Kein, Unbekannt
Autoren/Hrsg.

Herausgeber

Introduction. Experiences in the Inspecting of Quality Systems. GMP/ISO Quality Systems for Drug Products Manufacturers. Quality Management Systems & GMP. The Master Plan Concept. A Quality Manual for a Multinational Pharmaceutical Company. Implementation of a QA System into a German Pharmaceutical Company. Implementation of a Quality System. Experiences in the Auditing of QA Systems. How to Implement Validation into a QA System. How to Build a Supplier Qualification System. Hazard Analysis & Critical Control Points.