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OverviewMedical Devices Law and Regulation Answer Book walks you through the current regulatory requirements and provides in-depth coverage of individual FDA programs that cover everything from conducting clinical trials, preparing successful premarket submissions, adhering to quality system requirements, and fulfilling post-market obligations. With over thirty contributors from a variety of major law firms and consulting firms specializing in medical device work, Medical Devices Law and Regulation Answer Book provides practical guidance on how to handle everyday questions on a wide variety of topics, as well as what issues are likely to arise and how to avoid them. The Q&A guide also discusses related topics that have a marked impact on the medical devices industry, such as intellectual property, product liability, and reimbursement. Medical Devices Law and Regulation Answer Book is a practical in-depth reference for all lawyers, consultants, and companies operating in the medical devices sector, as well as all companies contemplating entry into the heavily regulated world of medical devices. Full Product DetailsAuthor: Susan Onel , Karen M. BeckerPublisher: Practising Law Institute Imprint: Practising Law Institute Edition: 2017 Edition Dimensions: Width: 15.10cm , Height: 5.30cm , Length: 23.00cm Weight: 1.439kg ISBN: 9781402427749ISBN 10: 1402427743 Pages: 1112 Publication Date: 01 November 2016 Audience: Professional and scholarly , Professional & Vocational Format: Paperback Publisher's Status: Active Availability: Available To Order ![]() We have confirmation that this item is in stock with the supplier. It will be ordered in for you and dispatched immediately. Table of ContentsReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |