Design Controls, Risk Management & Process Validation for Medical Device Professionals: A Comprehensive Handbook for Interpreting and Implementing Design Control Regulation
$147.98
Description
Book Synopsis: This handbook is ranked as a best seller and provides the most up to date resource currently available for interpreting and understanding design controls. This handbook is the most exhaustive resource ever written about FDA design controls for medical devices with a collection of all applicable regulations and real-world examples. Four-hundred & forty, 8.5" X 11" pages provides an extensive evaluation of FDA 21 CFR 820 and is cross-referenced with ISO 13485 to provide readers with a broad and in-depth review of practical design control implementation techniques. This handbook also covers basic, intermediate and advanced design control topics and is an ideal resource for implementing new design control processes or upgrading existing process into medical device quality systems. This critical resource also specifically outlines key topics which will allow quality managers and medical device developers to improve compliance quickly to pass internal and external audits and FDA inspections. The author breaks down the regulation line by line and provides a detailed interpretation by using supportive evidence from the FDA design control guidance and the quality systems preamble. Numerous examples, case studies, best practices, 70+ figures and 45+ tables provide practical implementation techniques which are based on the author's extensive experience launching numerous medical device products and by integrating industry consultant expertise. As an added bonus, web access to downloadable and editable design control documents are included with this purchase. In addition, bonus chapters include: explanation of medical device classification, compliance to design controls, risk management, and the design control quality system preamble. 30-50 pages are dedicated to each of the major design control topics: Design and Development Planning, Design Input, Design Output, Design Transfer, Design Verification, Design Validation, Design Change and Design History File.
Details
Looking for the most comprehensive and up-to-date resource on design controls for medical devices? Look no further than our best-selling handbook on Design Controls, Risk Management & Process Validation. With over four-hundred and forty pages of valuable content, this handbook is the ultimate guide for medical device professionals who want to interpret and implement design control regulations effectively.
What sets our handbook apart is its unique approach to providing a broad and in-depth review of practical design control implementation techniques. Our expert author has broken down the regulation line by line, offering a detailed interpretation backed by evidence from the FDA and quality systems preamble. This means you can confidently navigate through FDA inspections and audits while improving compliance quickly.
But the benefits don't stop there! Along with detailed explanations and real-world examples, this handbook also comes with web access to downloadable and editable design control documents. Our bonus chapters on medical device classification, compliance to design controls, risk management, and the design control quality system preamble further enhance the value you'll receive.
Upgrade your medical device quality systems today and ensure a smooth journey towards compliance and successful product launches. Don't miss out on this invaluable resource. Order your copy now and gain access to the knowledge and expertise that will set you apart from your competitors.
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