Sterile Manufacturing Regulations, Processes, and Guidelines

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Synopsis

This book highlights key ideas and factors to coach and guide professionals involved in learning about Sterile Manufacturing and operational requirements. It covers regulations and guidelines instituted by the FDA, ISPE, EMA, MHRA, and ICH, emphasizing good manufacturing practice and inspection requirements in the manufacturing of medicinal products.
 
Additionally, this book provides the fundamentals of aseptic techniques, quality by design, risk assessment, and management in support of sterile operations applications. It creates a link to the implementation of business practices in drug manufacturing and healthcare and forms a correlation between design strategies including a step-by-step process to ensure reliability, safety, and efficacy of healthcare products for human and animal use. The book also provides a connection between drug production and regulated applications by offering a review of the basic elements of sterile processing, and how to remain viable with solid strategic planning.
 
The book is a concise reference for professionals and learners in the field of sterile operations that governs primarily, pharmaceutical and medical device space, but can also extend to food and cosmetics that require clean (aseptic) manufacturing applications. It also helps compounding pharmacists and GMP inspectors and auditors.

Book details

Author:
Sam A. Hout
ISBN:
9781000406122
Related ISBNs:
9780367754358, 9781003162506, 9780367754372
Publisher:
CRC Press
Pages:
190
Reading age:
Not specified
Includes images:
Yes
Date of addition:
2021-07-04
Usage restrictions:
Copyright
Copyright date:
2022
Copyright by:
Sam A. Hout 
Adult content:
No
Language:
English
Categories:
Medicine, Nonfiction, Reference, Technology