Cleaning Validation ()
By Destin A. LeBlanc
By Destin A. LeBlanc
Pharmaceutical manufacturers and upper management are encouraged to meet the challenges of the science-based and risk-based approaches to cleaning validation. Using some of the principles and practices in this volume will help in designing a more effective and efficient cleaning validation program.
Features
- Timely coverage of cleaning validation for the pharmaceutical industry, a dynamic area in terms of health-based limits.
- The author encourages pharmaceutical manufacturers, and particularly upper management, to meet the challenges of the science-based and risk-based approaches to cleaning validation.
- Draws on the author’s vast experience in the field of cleaning validation and hazardous materials.
- Discusses EMA vs. ISPE on Cleaning Limits and revised Risk-MaPP for highly hazardous products in shared facilities.
- A diverse list of topics from protocol limits for yeasts and molds to cleaning validation for homeopathic drug products.
Product Details
- Publisher: CRC Press, December 2022
- Language: English
- ISBN: 9781000835595
Book Introduction
Are you a pharmaceutical manufacturer or part of the upper management team? If so, you are surely aware of the challenges that come with ensuring effective and efficient cleaning validation in your industry. Luckily, this book is here to help. In “Cleaning Validation for Pharmaceutical Manufacturers,” author Destin A. LeBlanc provides valuable insights and guidance on meeting the science-based and risk-based approaches to cleaning validation.
As the pharmaceutical industry evolves, so do the health-based limits that govern cleaning validation. This book offers timely coverage of this dynamic area, ensuring that you stay up to date with the latest information and regulations. LeBlanc emphasizes the importance of not only meeting these challenges but also encouraging upper management to do the same. By implementing the principles and practices outlined in this volume, you can design a more effective and efficient cleaning validation program for your organization.
Book Review
LeBlanc draws on his vast experience in the field of cleaning validation and hazardous materials to deliver a comprehensive guide. His expertise shines through in the depth and clarity of the information provided. From discussing the differences between EMA and ISPE on Cleaning Limits to exploring the revised Risk-MaPP for highly hazardous products in shared facilities, this book covers a diverse range of topics that are relevant to the pharmaceutical industry.
One of the standout features of this book is its practical approach. LeBlanc not only explains the theoretical concepts but also provides practical examples and case studies to illustrate their application. This makes it easier for readers to understand and implement the principles and practices discussed.
Promoting the Feeling of Ordering the Book or Video
If you are serious about improving the cleaning validation processes in your pharmaceutical manufacturing organization, “Cleaning Validation for Pharmaceutical Manufacturers” is a must-read. With its comprehensive coverage, practical approach, and emphasis on meeting the science-based and risk-based approaches, this book offers valuable insights and guidance.
By ordering this book, you gain access to the expertise and experience of Destin A. LeBlanc, a trusted authority in the field. Whether you are new to cleaning validation or looking to enhance your existing practices, this book provides the knowledge and tools you need to succeed.
Don’t miss out on the opportunity to optimize your cleaning validation program. Order “Cleaning Validation for Pharmaceutical Manufacturers” today and take your organization to the next level.
Product Details
- Publisher: CRC Press, December 2022
- Language: English
- ISBN: 9781000835595
- ISBN: 9781000835618