Biocontamination Control for Pharmaceutical and Healthcare - 1st Edition - ISBN: 9780128149119

Biocontamination Control for Pharmaceutical and Healthcare

1st Edition

Authors: Tim Sandle
Paperback ISBN: 9780128149119
Imprint: Academic Press
Published Date: 1st January 2019
Page Count: 250
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Description

Biocontamination control concerns the risks to medicinal products from microorganisms, microbial by-products, and particulates. The risks of biocontamination in a well-designed facility stem from transfer on people and material surfaces, airborne contamination, and via utilities and interfaces. Biocontamination Control for Pharmaceutical and Healthcare outlines elements in a biocontamination strategy that tracks through a facility with bio-burden control and reduction at each transition in classified areas; this is a key part of controlling risk escalation to contaminating medicinal products. Regulatory authorities have challenged pharmaceutical and healthcare sectors, and those involved in Good Manufacturing Practice (GMP), to adopt a holistic approach to contamination control. Established ways of assessing contamination are limited, and therefore risk-based approaches are required. As well as using risk to assess types of contamination and where contamination can arise, new technologies are needed to introduce barriers between personnel and the environment, and to provide a rapid and more accurate assessment of risk. This book offers guidance on building an up to date and complete biocontamination strategy.

Key Features

  • Provides the information for a facility to build a complete biocontamination strategy
  • Allows a facility to understand the main biocontamination risks to medicinal products
  • Assists the reader in navigating regulatory requirements and reducing process risks
  • Provides insight into developing an environmental monitoring programme
  • Covers the types of rapid microbiological monitoring methods now available, as well as current legislation

Readership

Researchers in pharmaceutical companies, pharmacies, biotechnology companies, graduate and postgraduate students in pharmaceuticals and healthcare; Engineers, pharmacologists, Quality Assurance personnel; Medical professionals, medical device specialists

Table of Contents

  1. Introduction
    2. Sources of microbial contamination and risk profiling
    3. GMP, regulations and standards
    4. Biocontamination control
    5. Introduction to cleanrooms and environmental monitoring
    6. Viable monitoring methods
    7. Selection of culture media
    8. Non-viable monitoring
    9. Rapid microbiological methods
    10. Designing an environmental monitoring programme
    11. Special Types of Environmental Monitoring
    12. Cleanrooms and microflora
    13. Assessment of pharmaceutical water systems
    14. Data handling and trend analysis
    15. Bioburden and endotoxin assessment of pharmaceutical processing
    16. Risk assessment and investigation for environmental monitoring
    17. Assessing and removing contamination risks from the process
    18. The human factor
    19. Biocontamination deviation management

Details

No. of pages:
250
Language:
English
Copyright:
© Academic Press 2019
Published:
Imprint:
Academic Press
Paperback ISBN:
9780128149119

About the Author

Tim Sandle

Tim Sandle is a chartered biologist and holds a first class honours degree in Applied Biology, a Master’s degree in education, and a doctorate from Keele University in the UK. Tim has over 25 years’ experience of microbiological research and biopharmaceutical processing. This includes experience of designing, validating and operating a range of microbiological tests. In addition, Tim is experienced in pharmaceutical microbiological risk assessment and investigation. Tim serves on several national and international committees relating to pharmaceutical microbiology and cleanroom contamination control (including the ISO cleanroom standards). He is a committee member of the Pharmaceutical Microbiology Interest Group (Pharmig); serves on the National Blood Service advisory cleaning and disinfection committee; and is a member of several editorials boards for scientific journals. Tim has written over 400 book chapters, peer reviewed papers and technical articles relating to microbiology.

Affiliations and Expertise

Head of Microbiology, Bio Products Laboratory, Elstree, UK and Visiting Tutor, School of Pharmacy and Pharmaceutical Sciences, Manchester University, UK

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