Research Catalog
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Displaying 1-19 of 19 results
Combination products : regulatory challenges and successful product developement / Smita Gopalaswamy, Venky Gopalaswamy.
- Text
- Boca Raton : CRC Press, c2008.
- 2008
- 1 Item
Item details Format Call Number Item Location Text JBE 08-1347 Schwarzman Building - General Research Room 315 Available - Can be used on site. Please visit New York Public Library - Schwarzman Building to submit a request in person.
Development of FDA-regulated medical products : prescription drugs, biologics, and medical devices / Elaine Whitmore.
- Text
- Milwaukee, Wis. : ASQ Quality Press, [2004], ©2004.
- 2004-2004
- 2 Items
Item details Format Call Number Item Location Text Off-site Not available - Please for assistance.Item details Format Call Number Item Location Text RA401.5 .W48 2004 Off-site Not available - Please for assistance.Clinical evaluation of medical devices : principles and case studies / edited by Karen Becker Witkin.
- Text
- Totowa, N.J. : Humana Press, [1998], ©1998.
- 1998-1998
- 1 Item
Item details Format Call Number Item Location Text R856 .C545 1998 Off-site Medical device safety : the regulation of medical devices for public health and safety / Gordon R. Higson.
- Text
- 2002
- 1 Item
Item details Format Call Number Item Location Text R856.6 .H53 2002 Off-site Medical device regulations : global overview and guiding principles.
- Text
- 2003
- 1 Item
Item details Format Call Number Item Location Text R856.6 .M445 2003 Q Off-site Six Sigma for medical device design / Jose Justiniano, Venky Gopalaswamy.
- Text
- Boca Raton, FL : CRC Press, [2005], ©2005.
- 2005-2005
- 1 Item
Item details Format Call Number Item Location Text R856.6 .J876 2005 Off-site Clinical evaluation of medical devices / edited by Karen M. Becker, John J. Whyte.
- Text
- Totowa, N.J. : Humana Press, [2006], ©2006.
- 2006-2006
- 2 Items
Item details Format Call Number Item Location Text Off-site Not available - Please for assistance.Item details Format Call Number Item Location Text R856 .C545 2006 Off-site Combination products : regulatory challenges and successful product developement / Smita Gopalaswamy, Venky Gopalaswamy.
- Text
- Boca Raton : CRC Press, [2008], ©2008.
- 2008-2008
- 1 Item
Item details Format Call Number Item Location Text RM301.27 .G68 2008 Off-site Development and approval of combination products : a regulatory perspective / edited by Evan B. Siegel.
- Text
- Hoboken, N.J. : Wiley, [2008], ©2008.
- 2008-2008
- 2 Items
Item details Format Call Number Item Location Text Off-site Not available - Please for assistance.Item details Format Call Number Item Location Text RA401.5 .D48 2008 Off-site Design, execution, and management of medical device clinical trials / Salah Abdel-aleem.
- Text
- 2009
- 1 Item
Item details Format Call Number Item Location Text R856.4 .A23 2009 Off-site A clinical trials manual from the Duke Clinical Research Institute : lessons from a horse named Jim / Margaret B. Liu and Kate Davis.
- Text
- 2010
- 2 Items
Item details Format Call Number Item Location Text Off-site Not available - Please for assistance.Item details Format Call Number Item Location Text R853.C55 L58 2010 Off-site The design and management of medical device clinical trials : strategies and challenges / Salah Abdel-aleem.
- Text
- Hoboken, N.J. : John Wiley, c2010.
- 2010
- 1 Item
Item details Format Call Number Item Location Text R856.4 .A22 2010 Off-site Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report / Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies.
- Text
- Washington, D.C. : National Academies Press, [2010], ©2010.
- 2010-2010
- 1 Item
Item details Format Call Number Item Location Text RA399.A3 P83 2010g Off-site Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report / Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies.
- Text
- Washington, D.C. : National Academies Press, [2010], ©2010.
- 2010
- 1 Item
Item details Format Call Number Item Location Text RA399.A3 P83 2010g Off-site The regulation of medical products / edited by J.P. Griffin and J. O'Grady.
- Text
- London : BMJ Books, 2003.
- 2003
- 1 Item
Item details Format Call Number Item Location Text K3636 .R44 2003 Off-site The FDA and worldwide quality system requirements guidebook for medical devices / compiled and written by Amiram Daniel & Ed Kimmelman.
- Text
- Milwaukee, Wis. : ASQ Quality Press, 2008.
- 2008
Redirecting innovation in U.S. health care : options to decrease spending and increase value / Steven Garber [and six others].
- Text
- Santa Monica, CA : Rand Corporation, [2014]
- 2014-2014
- 1 Item
Item details Format Call Number Item Location Text RA410.53 .G36 2014 Off-site Current issues in human subject protection : an FDA perspective : September 13, 1996, Natcher Auditorium.
- Text
- [Rockville, MD] : Food and Drug Administration, [1996?]
- 1996
- 1 Item
Item details Format Call Number Item Location Text HE 20.4002:H 88 Off-site Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report / Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies.
- Text
- Washington, D.C. : National Academies Press, [2010], ©2010.
- 2010-2010
- 1 Item
Item details Format Call Number Item Location Text RA399.A3 P83 2010 Off-site
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