9781119356073-1119356075-Pharmaceutical Microbiological Quality Assurance and Control: Practical Guide for Non-Sterile Manufacturing

Pharmaceutical Microbiological Quality Assurance and Control: Practical Guide for Non-Sterile Manufacturing

ISBN-13: 9781119356073
ISBN-10: 1119356075
Edition: 1
Author: David Roesti, Marcel Goverde
Publication date: 2020
Publisher: Wiley
Format: Hardcover 592 pages
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Book details

ISBN-13: 9781119356073
ISBN-10: 1119356075
Edition: 1
Author: David Roesti, Marcel Goverde
Publication date: 2020
Publisher: Wiley
Format: Hardcover 592 pages

Summary

Pharmaceutical Microbiological Quality Assurance and Control: Practical Guide for Non-Sterile Manufacturing (ISBN-13: 9781119356073 and ISBN-10: 1119356075), written by authors David Roesti, Marcel Goverde, was published by Wiley in 2020. With an overall rating of 3.9 stars, it's a notable title among other Industrial, Manufacturing & Operational Systems (Engineering) books. You can easily purchase or rent Pharmaceutical Microbiological Quality Assurance and Control: Practical Guide for Non-Sterile Manufacturing (Hardcover) from BooksRun, along with many other new and used Industrial, Manufacturing & Operational Systems books and textbooks. And, if you're looking to sell your copy, our current buyback offer is $3.2.

Description

Relying on practical examples from the authors’ experience, this book provides a thorough and modern approach to controlling and monitoring microbial contaminations during the manufacturing of non-sterile pharmaceuticals.

Offers a comprehensive guidance for non-sterile pharmaceuticals microbiological QA/QC Presents the latest developments in both regulatory expectations and technical advancements Provides guidance on statistical tools for risk assessment and trending of microbiological data Describes strategy and practical examples from the authors’ experience in globalized pharmaceutical companies and expert networks

  • Offers a comprehensive guidance for non-sterile pharmaceuticals microbiological QA/QC
  • Presents the latest developments in both regulatory expectations and technical advancements
  • Provides guidance on statistical tools for risk assessment and trending of microbiological data
  • Describes strategy and practical examples from the authors’ experience in globalized pharmaceutical companies and expert networks
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