eBook, PDF

Pharmaceutical Manufacturing Handbook (eBook, PDF)

Regulations and Quality

Redaktion: Gad, Shayne Cox

Beschreibung

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.

Technische Details

• Geräte: PC
• mit Kopierschutz
• Größe: 8.54MB

Barrierefreiheit

• Text-to-Speech

Autor

SHAYNE COX GAD, PhD, DABT, ATS, is the Principal of Gad Consulting Services. Dr. Gad has more than thirty years of experience as a toxicologist, statistical consultant, manager, and general consultant on research and development in the chemical, consumer product, contract testing, biotechnology, medical device, and pharmaceutical industries. He is the author of twenty-nine books and numerous papers, presentations, and other publications.

Produktdetails

• Verlag: Wiley
• Seitenzahl: 856
• Erscheinungstermin: 13. März 2008
• Englisch
• ISBN-13: 9780470259825
• Artikelnr.: 37291550

Rezensionen

This book is a valuable reference .The book contains everything you need to ensure full compliance and superior quality control. ( Pharmaceutical Technology Magazine , July 2, 2008)