Author: Carol V. Desain
Edition: 2
Publisher: CRC Press
Binding: Hardcover
ISBN: 1574910639
Validation for Medical Device and Diagnostic Manufacturers, Second Edition
Implementation of FDA's Design Control requirements (21 CFR 820. Medical books Validation for Medical Device and Diagnostic Manufacturers, Second Edition. 0) changed an entire industry. Quality System Requirements defined the approach to medical device validation. Product design, manufacturing process, and test method validation studies must be performed before or as a product is transferred to commercial production. Validation studies must demonstrate that product design, process, and test methods/requirements/specifications determined during development can be met in the environment of intended use Medical books Validation For Medical Device And Diagnostic Manufacturers, Second Edition Carol. author carol v desain author charmaine v sutton format hardback language english publication year 30 09 1997 subject family health relationships subject 2 family health general title validation for medical device and diagnostic manufacturers second edition author carol v desain charmaine v sutton publisher informa healthcare publication date sep 01 1997 pages 332 binding hardcover edition 2 nd dimensions 6 25 wx 9 50 hx 0 75 d isbn 1574910639 subject medical general brand new hardcover all ord
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author carol v desain author charmaine v sutton format hardback language english publication year 30 09 1997 subject family health relationships subject 2 family health general title validation for medical device and diagnostic manufacturers second edition author carol v desain charmaine v sutton publisher informa healthcare publication date sep 01 1997 pages 332 binding hardcover edition 2 nd dimensions 6 25 wx 9 50 hx 0 75 d isbn 1574910639 subject medical general brand new hardcover all ord
"Implementation of FDA's Design Control requirements (21 CFR 820.30) changed an entire industry. Quality System Requirements defined the approach to medical device validation. Product design, manufacturing process, and test method validation studies must be performed before or as a product is transferred to commercial production. Validation studies must demonstrate that product design, process, and test methods/requirements/specifications determined during development can be met in the environment of intended use. This book provides practical guidance on how to develop and validate product des
"Implementation of FDA's Design Control requirements (21 CFR 820.30) changed an entire industry. Quality System Requirements defined the approach to medical device validation. Product design, manufacturing process, and test method validation studies must be performed before or as a product is transferred to commercial production. Validation studies must demonstrate that product design, process, and test methods/requirements/specifications determined during development can be met in the environment of intended use. This book provides practical guidance on how to develop and validate product des
"Implementation of FDA's Design Control requirements (21 CFR 820.30) changed an entire industry. Quality System Requirements defined the approach to medical device validation. Product design, manufacturing process, and test method validation studies must be performed before or as a product is transferred to commercial production. Validation studies must demonstrate that product design, process, and test methods/requirements/specifications determined during development can be met in the environment of intended use. This book provides practical guidance on how to develop and validate product des
Medical Book Validation for Medical Device and Diagnostic Manufacturers, Second Edition
0) changed an entire industry. Quality System Requirements defined the approach to medical device validation. Product design, manufacturing process, and test method validation studies must be performed before or as a product is transferred to commercial production. Validation studies must demonstrate that product design, process, and test methods/requirements/specifications determined during development can be met in the environment of intended use. This book provides practical guidance on how to develop and validate product designs, manufacturing processes, and test methods that comply with the requirements of QSR.
