Read more
Informationen zum Autor Charmaine V. Sutton, Carol V. Desain Klappentext 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 designs, manufacturing processes, and test methods that comply with the requirements of QSR. Zusammenfassung 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 designs! manufacturing processes! and test methods that comply with the requirements of QSR. Inhaltsverzeichnis Introduction to Quality Systems. Validation Overview. Product Development & Validation. Validation Study Plans, Protocols, Reports. Process Development & Validation. Test Method Development & Validation. Qualification of Equipment & Equipment Systems. Qualification of Software-Driven, Automated Equipment & Equipment Systems. Facility Qualification Studies. Validation Studies at Suppliers & Contractors. Change Management for Validated Products, Processes, & Methods. Revalidation & Requalification Studies. Supporting Appendices....
