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By: (Author) Professor Sarfaraz K. Niazi , (Author) Sunitha Lokesh
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This volume covers theregulatory processes involved in producing a GMP (Good Manufacturing Practice) biopharmaceuticalproduct for commercial distribution, including areas of current GMP,registration, and legal and ethical considerations. Emerging trends in thetechnology and regulatory compliance are also discussed, with advice onestablishing efficient manufacturing facilities. Intended for practitioners in the commercial biopharmaceuticalmanufacturing industry, the text is an ideal resource for practitioners lookingto develop their ability to manufacture biopharmaceutical products at a largescale.
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