Shulph Ink
Good Design Practices for GMP Pharmaceutical Facilities
Good Design Practices for GMP Pharmaceutical Facilities
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Excellent- More about Good Design Practices for GMP Pharmaceutical Facilities
This revised publication is a valuable resource for professionals involved in planning, designing, building, validating, and maintaining modern cGMP pharmaceutical manufacturing facilities in the U.S. and internationally, focusing on facility planning, sustainability, and LEED building ratings.
Format: Paperback / softback
Length: 536 pages
Publication date: 13 June 2022
Publisher: Taylor & Francis Ltd
This revised publication serves as a comprehensive and up-to-date resource for professionals involved in the planning, design, construction, validation, and maintenance of modern cGMP pharmaceutical manufacturing facilities in the United States and internationally. The new edition expands on facility planning, particularly emphasizing the growing necessity to modify existing legacy facilities, and also addresses current trends in pharmaceutical manufacturing, including strategies for sustainability and LEED building ratings. All chapters have undergone a thorough re-examination with a fresh perspective on current good design practices.
Introduction
Purpose of the Publication
Key Features of the Publication
Facility Planning
Design Considerations
Construction and Commissioning
Validation and Maintenance
Conclusion
Dimension: 254 x 178 (mm)
ISBN-13: 9781032339962
Edition number: 2 ed
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