Design Controls for the Medical Device Industry

Revised
ISBN: 978-1-4665-0354-0
Verlag: CRC PR INC

Buch, Englisch, 205 Seiten, Format (B × H): 154 mm x 241 mm, Gewicht: 488 g

The second edition of a bestseller, Design Controls for the Medical Device Industry provides a comprehensive review of the latest design control requirements, as well as proven tools and techniques to ensure your company’s design control program evolves in accordance with current industry practice. The text assists in the development of an effective design control program that not only satisfies the US FDA Quality System Regulation (QSR) and ISO 9001 and 13485 standards, but also meets today’s third-party auditor/investigator expectations and saves you valuable time and money.
The author’s continual participation in FDA QSR inspections and Notified Body ISO audits is reflected in updates to all chapters and appendices of the book, now bursting at the seams with:

New coverage of ISO 9001 and 13485 design control requirements
More real-world examples from the medical device industry
Additional detail for greater understanding and clarity
Fresh templates for practical implementation
Extensive references for further study

The book addresses design control elements such as design planning, input, output, review, verification, validation, change, transfer, and history, as well as risk management inclusive of human factors and usability, biocompatibility, the FDA Quality System Inspection Technique (QSIT) for design controls, and medical device regulations and classes in the US, Canada, and Europe.

Zielgruppe

Practitioners in the medical device industry and graduate students in medical device design.

Autoren/Hrsg.

Teixeira, Marie B.

Inhaltsverzeichnis

Preface
Author Biography
Introduction
Device Classification
Overview of Design Controls
Design and Development Planning
Design Inputs Part I
Design Inputs Part II
Design Outputs
Design Review
Design Verification
Risk Management
Design Validation
Biocompatibility
Design Transfer
Design Change
Design History File
Quality System Inspection Technique
References
Appendix A – Design Controls Procedure

Appendix B – Product Performance Specification

Appendix C – Product Claims Sheet

Appendix D – Design Input/Output Matrix

Appendix E – Project Approval Form

Appendix F – Design Review Meeting Record Template

Appendix G – Risk Management Plan Template

Appendix H – Clinical Evaluation Report Template

Appendix I – Design Transfer Checklist

Appendix J – Design Change Form Template

Appendix K – Approval for Sale Template

Index

Über Autor(innen)

Marie B. Teixeira is founder and principal consultant for QA/RA Compliance Connection, Inc., Odessa, Florida, USA. She holds a BS from University of Massachusetts Amherst, USA and is an American Society for Quality member, ASQ-certified quality manager and engineer, and RABQSA principle auditor. Previously she served as quality engineer at Raytheon, Norwood, Massachusetts, USA; GTE Government Systems, Needham Heights, Massachusetts, USA; and Sparton Electronics, Brooksville, Florida, USA; as well as director of quality assurance and regulatory affairs at Bioderm, Inc., Tampa Bay, Florida, USA and quality systems manager for regulatory affairs at Smith & Nephew, Largo, Florida, USA.