The FDA and Worldwide Current Good Manufacturing Practices and Quality System Requirements Guidebook for Finished Pharmaceuticals

The FDA and Worldwide Current Good Manufacturing Practices and Quality System Requirements Guidebook for Finished Pharmaceuticals
Author: José Rodríguez Pérez
Publisher:
Total Pages: 369
Release: 2014
Genre: Drugs
ISBN: 9781680157840

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The FDA and Worldwide Current Good Manufacturing Practices and Quality System Requirements Guidebook for Finished Pharmaceuticals
Language: en
Pages: 369
The FDA and Worldwide Current Good Manufacturing Practices and Quality System Requirements Guidebook for Finished Pharmaceuticals
Language: en
Pages: 260
Authors: José (Pepe) Rodríguez-Pérez
Categories: Business & Economics
Type: BOOK - Published: 2014-04-30 - Publisher: Quality Press

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Good Manufacturing Practices (GMP) for human pharmaceuticals affects every patient taking a medicine. GMP covers all aspects of the manufacturing process, from
The FDA and Worldwide Quality System Requirements Guidebook for Medical Devices
Language: en
Pages: 355
Authors: Amiram Daniel
Categories: Medical
Type: BOOK - Published: 2008-01-01 - Publisher: Quality Press

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How have recent changes in domestic and international regulations affected quality management in the development and marketing of medical devices in the US and
Good Manufacturing Practices for Pharmaceuticals
Language: en
Pages: 418
Authors: Joseph D. Nally
Categories: Medical
Type: BOOK - Published: 2016-04-19 - Publisher: CRC Press

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With global harmonization of regulatory requirements and quality standards and national and global business consolidations ongoing at a fast pace, pharmaceutica
The FDA and Worldwide Current Good Manufacturing Practices and Quality System Requirements Guidebook for Finished Pharmaceuticals
Language: en
Pages: 246
Authors: José Rodríguez-Pérez
Categories: Business & Economics
Type: BOOK - Published: 2014-08-15 - Publisher: Quality Press

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This guidance book is meant as a resource to manufacturers of pharmaceuticals, providing up-to-date information concerning required and recommended quality syst