My Account Log in

6 options

Medical device software verification, validation and compliance / David A. Vogel.

EBSCOhost Academic eBook Collection (North America) Available online

View online

EBSCOhost Ebook Medical Collection Available online

View online

EBSCOhost eBook Community College Collection Available online

View online

Ebook Central Academic Complete Available online

View online

Knovel Biochemistry, Biology & Biotechnology Academic Available online

View online

eBook EngineeringCore Collection Available online

View online
Format:
Book
Author/Creator:
Vogel, David A.
Language:
English
Subjects (All):
Medical instruments and apparatus--Testing.
Medical instruments and apparatus.
Biomedical engineering.
Physical Description:
1 online resource (444 p.)
Edition:
1st ed.
Place of Publication:
Norwood, MA : Artech House, 2010.
Language Note:
English
Summary:
Here's 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 software's 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, and in compliance with regulations. Additionally, an entire part of the book is devoted to the validation of software that automates any part of a manufacturer's quality system and is regulated by 21 CFR 820.70(i). DVD Included! Contains a collection of FDA regulations and guidance documents related to software in the medical device industry, valuable sample forms and templates, and supplemental figures that support key topics covered in the book. Publisher abstract.
Contents:
Machine generated contents note: pt. I Background
ch. 1 Evolution of Medical Device Software Validation and the Need for This Book
Evolution of Validation in the Medical Device Industry
Building a Language to Discuss Validation
Terminology is the Foundation
Correct Versus Consistent Terminology
Terminology Need Not Be Entertaining
Notes:
Print version record.
Includes bibliographical references and index.
Includes index.
ISBN:
1-5231-1739-7
1-59693-423-9
OCLC:
694729137

The Penn Libraries is committed to describing library materials using current, accurate, and responsible language. If you discover outdated or inaccurate language, please fill out this feedback form to report it and suggest alternative language.

My Account

Shelf Request an item Bookmarks Fines and fees Settings

Guides

Using the Library Catalog Using Articles+ Library Account