HereOCOs the first book written specifically to help medical device and software engineers, QA and compliance professionals, and corporate business managers better understand and implement critical verification and validation processes for medical device software.Offering you a much broader, higher-level picture than other books in this field, this book helps you think critically about software validation -- to build confidence in your softwareOCOs safety and effectiveness. The book presents validation activities for each phase of the development lifecycle and shows: why these activities are important and add value; how to undertake them; and what outputs need to be created to document the validation process.From software embedded within medical devices, to software that performs as a medical device itself, this comprehensive book explains how properly handled validation throughout the development lifecycle can help bring medical devices to completion sooner, at higher quality, in compliance with regulations."
After reading this book, new testers will have a solid foundation on which to start their careers on, and experienced testers will be able to identify inconsistencies and myths within their current test practices.
"Acquaints developers of medical devices with the basic concepts and major issues of medical quality assurance and regulatory documents, describes the requirements listed in these documents, and provides strategies for compliance with these ...
This book, which is relevant to the pharmaceutical and medical devices regulated operations, provides practical information to assist in the computer validation to production systems, while highlighting and efficiently integrating worldwide ...
This handbook provides the most up to date resource currently available for interpreting and understanding design controls.
As such, a company's design control program should be dynamic in nature and continue to evolve in accordance with current standards and industry practice. It is hard to believe that it has been over 16 years since the book was first ...
Ensuring that organizations transition smoothly to the new system, this guide explains how to implement the new GMP paradigm while maintaining continuity with current practices.
... software validation is " confirmation by examination and provision of ... verification and validation by listing and discussing their respective ... device software , irrespective of its device class , is subject to applicable design ...
... medical device software assessment method. A pilot MDevSPICE-Adept ... compliance requirements with specific standards. Given the level of demand ... Validation; Final Guidance for Industry and FDA Staff. CDRH: Rockville (2002) 6. US FDA ...
... Medical device regulation: an introduction for the practicing physician ... Software and Systems. Computer 39(4), 33–38 (2006) 3. Abraham, C., Nishiharas, E ... Verification, Validation and Compliance. Artech House, Norwood (2010) IEC ...
The intent of this book is to provide manufacturing quality professionals working in virtually any industry a quick, convenient, and comprehensive guide to properly conduct process validations that meet regulatory and certification ...