Author: José Rodríguez-Pérez
Edition:
Publisher: Quality Press
Binding: Hardcover
ISBN: 0873897978
CAPA for the FDA-Regulated Industry
Medical devices, biopharmaceutical, and traditional drug manufacturing companies devote an important part of their resources to dealing with incidents, investigations, and corrective and preventive actions. Medical books CAPA for the FDA-Regulated Industry. The corrective and preventive action system is known as the CAPA system. It is second to none in terms of frequency and criticality of its deviations, and most of the regulatory actions taken by the FDA and foreign regulators are linked to inadequate CAPA systems. This guidance book provides useful and up-to-date information about this critical topic to thousands of engineers, scientists, and manufacturing and quality personnel across the life sciences industries. Understanding and improving the CAPA system as a whole is the focal point of this book, the first of its kind dealing exclusively with this critical system within this highly regulated industry Medical books CAPA for the FDA-Regulated Industry, 9780873897976. CAPA for the FDA-Regulated Industry, ISBN-13: 9780873897976, ISBN-10: 0873897978
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CAPA for the FDA-Regulated Industry, ISBN-13: 9780873897976, ISBN-10: 0873897978
Powered by Frooition Pro Click here to view full size. Full Size Image Click to close full size. CAPA for the FDA-Regulated Industry - Book NEW Author(s): Jose Rodriguez-perez Format: Hardcover # Pages: 147 ISBN-13: 9780873897976 Published: 10/15/2010 Language: English Weight: 0.85 pounds Brand new book. About Us Payment Shipping Customer Service FAQs Welcome to MovieMars All items are Brand New. We offer unbeatable prices, quick shipping times and a wide selection second to none. Purchases com
Categories: Manufacturing industries, Quality Control * General, Business * Decision Making & Problem Solvin. Contributors: José Rodríguez-Pérez - Author. Format: NOOK Book
The CAPA (corrective and preventive action) system is the means by which medical device, biopharmaceutical, and drug manufacturing companies deal with and seek to prevent problem incidents and inadequate CAPA systems are the reasons for most of the regulatory actions taken by the Food and Drug Administration. This text provides guidance to engineers, scientists, and manufacturing and quality personnel across the life sciences industries on understanding, developing, implementing, documenting, and improving a CAPA system and includes forms that can be used as templates for failure investigation
Medical Book CAPA for the FDA-Regulated Industry
The corrective and preventive action system is known as the CAPA system. It is second to none in terms of frequency and criticality of its deviations, and most of the regulatory actions taken by the FDA and foreign regulators are linked to inadequate CAPA systems. This guidance book provides useful and up-to-date information about this critical topic to thousands of engineers, scientists, and manufacturing and quality personnel across the life sciences industries. Understanding and improving the CAPA system as a whole is the focal point of this book, the first of its kind dealing exclusively with this critical system within this highly regulated industry. By helping those in this industry improve their CAPA systems, it will be a crucial aid in their mission of producing safe and effective products.
