Good Design Practices for GMP Pharmaceutical Facilities
Good Design Practices for GMP Pharmaceutical Facilities by Terry Jacobs is a comprehensive resource published by CRC Press in 2016. This 2nd edition, comprising 516 pages, serves as a current reference for professionals involved in the planning, design, construction, validation, and maintenance of modern cGMP pharmaceutical manufacturing facilities both in the U.S. and internationally.
Readers will find an expanded focus on facility planning, particularly addressing the need to modify existing legacy facilities. The book discusses current trends in pharmaceutical manufacturing, including strategies for sustainability and LEED building ratings. Each chapter has been thoroughly re-examined to reflect contemporary good design practices, making this edition a valuable tool for those in the pharmaceutical and biotechnology industries.
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This revised publication serves as a handy and current reference for professionals engaged in planning, designing, building, validating and maintaining modern cGMP pharmaceutical manufacturing facilities in the U.S. and internationally. The new edition expands on facility planning, with a focus on the ever-growing need to modify existing legacy facilities, and on current trends in pharmaceutical manufacturing which include strategies for sustainability and LEED building ratings. All chapters have been re-examined with a fresh outlook on current good design practices.
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