Author: Jonathan S. Kahan
Edition: 2nd
Binding: Hardcover
ISBN: 1882615921
Edition: 2nd
Binding: Hardcover
ISBN: 1882615921
Medical Device Development: Regulation and Law
Medical Device Development: Regulation and Law, 2nd Edition, is the must-have resource for the novice or veteran medical device regulatory affairs professional.
by Kahan - Barnett International (2009) - Hardback - ISBN 1882615921 9781882615926
This practical reference provides the most comprehensive and updated analysis of US medical device and diagnostics development and approval requirements anywhere. This book also features in-depth analysis on how emerging developments and trends are reshaping medical device and combination product regulations in the US. The second edition of this popular and authoritative resource addresses the latest regulatory and legal developments that guide how medical devices are developed today: * The Medical Device User Fee and Modernization Act of 2002, including user fees, third party inspections,
Medical Device Development: Regulation and Law, 9781882615926
Medical Device Development: Regulation and Law, ISBN-13: 9781882615926, ISBN-10: 1882615921
format hardback language english publication year 13 07 2011 subject medicine subject 2 medical nursing ancillary services title creating 21 st century medical devices development needs and issues author parker nelson e editor publisher nova science pub inc publication date mar 30 2011 pages 206 binding hardcover edition 1 st dimensions 7 25 wx 10 00 hx 0 75 d isbn 1608767736 subject medical research brand new hardcover all orders get full access to our online status tracking service allowing
format hardback language english publication year 13 07 2011 subject medicine subject 2 medical nursing ancillary services title creating 21 st century medical devices development needs and issues author parker nelson e editor publisher nova science pub inc publication date mar 30 2011 pages 206 binding hardcover edition 1 st dimensions 7 25 wx 10 00 hx 0 75 d isbn 1608767736 subject medical research brand new hardcover all orders get full access to our online status tracking service allowing
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This practical reference provides the most comprehensive and updated analysis of US medical device and diagnostics development and approval requirements anywhere
The second edition of this popular and authoritative resource addresses the latest regulatory and legal developments that guide how medical devices are developed today: * The Medical Device User Fee and Modernization Act of 2002, including user fees, third party inspections,
