Description:
Parexel International, 2009. Hardcover. Good Condition/No Dust Jacket. Size: 8mo - over 7 3/4" - 9 3/4" tall. 546 pp. Text contains minor marks and annotations. Previous owner's name on bottom edge. Minimal shelfwear to the cover. Quantity Available: 1. Shipped Weight: 2 - 3 pounds. Category: Business, Finance & Marketing; Medicine & Health. ISBN: 1882615921. ISBN/EAN: 9781882615926. Pictures of this item not already displayed here available upon request. Inventory No: 113107. . 9781882615926 Additional shipping charges may apply.
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Medical Device Development: Regulation and Law Hardcover - 2009
by Kahan, Jonathan S.
Details
- Title Medical Device Development: Regulation and Law
- Author Kahan, Jonathan S.
- Binding Hardcover
- Edition 2nd
- Pages 550
- Publisher Parexel Intl Corp
- Date 2009-08
- ISBN 9781882615926
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Medical Device Development: Regulation and Law
by Jonathan S. Kahan
- Used
- Hardcover
- Condition
- Used - Good Condition
- Binding
- Hardcover
- ISBN 10 / ISBN 13
- 9781882615926 / 1882615921
- Quantity Available
- 1
- Seller
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Oak Point, Texas, United States
- Item Price
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€85.19€4.73 shipping to USA
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€85.19
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MEDICAL DEVICE DEVELOPMENT: REGULATION AND LAW
by KAHAN, JONATHAN S. & hartson, hogan llp
- Used
- very good
- Hardcover
- Condition
- Used - Very Good
- Edition
- Second Edition"
- Binding
- Hardcover
- ISBN 10 / ISBN 13
- 9781882615926 / 1882615921
- Quantity Available
- 1
- Seller
-
Durham, California, United States
- Item Price
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€141.99€3.31 shipping to USA
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Description:
Parexel Intl Corp. Very Good. 2009. Second Edition". Hardcover. 9.4 X 6.5 X 1.6 inches. VERY GOOD CONDITION, I noticed 3 sentences yellow hilited, ow it is solid,bright, appears to be unread ; WHITE TITLES ON black HARD COVERS, showing 3 photos and large x ray view of electronic implant ; 550 pages; The design and functional complexity of medical devices and systems has increased during the past half century, evolving from the level of cardiac pacemakers to magnetic resonance imaging devices. Such life-saving advancements are monumentally advantageous, but with so much at stake, regulation & laws are inevitable. 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, reprocessed single use devices, and the establishment of the Office of Combination Products. * The Food and Drug Administration Amendments Act of 2007, including unique device…
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€141.99
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