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Quality Risk Management in the FDA-Regulated Industry
Language: en
Pages: 252
Authors: José Rodríguez-Pérez
Categories: Business & Economics
Type: BOOK - Published: 2017-02-21 - Publisher: Quality Press

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The purpose of this new edition is to offer an updated view of the risk management field as it applies to medical products. Since the publication of the first e
Quality Risk Management in the FDA-Regulated Industry
Language: en
Pages: 313
Authors: Jose (Pepe) Rodriguez-Perez
Categories: Business & Economics
Type: BOOK - Published: 2024-04-18 - Publisher: Quality Press

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For quality professionals and manufacturers in the food safety and medical device industries, risk management is essential to ensuring organizations meet FDA re
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
Designing A World-Class Quality Management System For FDA Regulated Industries
Language: en
Pages: 136
Authors: David N. Muchemu
Categories: Business & Economics
Type: BOOK - Published: 2008-04-07 - Publisher: AuthorHouse

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Having a robust and functional Quality Management system is a QSR requirement for all Pharmaceutical,Biomedical,and Medical Device companies.This book does the
Foundations of Quality Risk Management
Language: en
Pages: 340
Authors: Jayet Moon
Categories: Business & Economics
Type: BOOK - Published: 2022-10-22 - Publisher: Quality Press

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In today's uncertain times, risk has become the biggest part of management. Risk management is central to the science of prediction and decision-making; holisti