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A delicate balance FDA and the reform of the medical device approval process : hearing before the Sp

United States. Congress. Senate. Special Committee on Aging.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., U.S. G.P.O., 2011. 2011

Discussion draft of the Food and Drug Administration Globalization Act legislation device and cosmet

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2008. 2008

Ensuring safe medicines and medical devices for children : hearing of the Committee on Health, Educa

United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2008. 2008

The impact of medical device and drug regulation on innovation, jobs, and patients a local perspecti

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2012. 2012

Mastering and managing the FDA maze : medical device overview, a training and management desk refere

Harnack, Gordon, 1939- author.
Milwaukee, Wisconsin : ASQ Quality Press, [2014] 2014

Medical device design and regulation

DeMarco, Carl T., author.
Milwaukee, Wisconsin : ASQ Quality Press, 2011. 2011

Medical device regulation too early to assess European system's value as model for FDA : report to t

United States. General Accounting Office.
Washington, D.C. : The Office ; Gaithersburg, MD (P.O. Box 6015, Gaithersburg 20884-6015) : The Office [distributor, 1996] 1996

Medical device regulation : FDA-CDRH manufacturing, policies and regulation handbook

Wreh, Elijah.
London, United Kingdom ; San Diego, CA, United States ; Cambridge, MA, United States ; Kidlington, Oxford, United Kingdom : Elsevier, Academic Press, an Imprint of Elsevier, [2023] 2023

Medical device reporting improvements needed in FDA's system for monitoring problems with approved d

United States. General Accounting Office.
Washington, D.C. : The Office ; Gaithersburg, MD (P.O. Box 6015, Gaithersburg 20884-6015) : The Office [distributor, 1997] 1997

Medical device safety : how FDA regulates the reprocessing of supposedly single-use devices : hearin

United States. Congress. House. Committee on Government Reform.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2006. 2006

Medical devices and the public's health the FDA 510(k) clearance process at 35 years

Institute of Medicine (U.S.)
Washington, D.C. : National Academies Press, 2011. 2011

Medical devices are current regulations doing enough for patients? : hearing before the Subcommittee

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2012. 2012

Medical devices FDA can improve oversight of tracking and recall systems : report to the Subcommitte

United States. General Accounting Office.
Washington, D.C. (P.O. Box 37050, Washington 20013) : U.S. General Accounting Office, [1998] 1998

Medical product innovation and regulation : benefits and risks

Bodie, Agata, author.
[Washington, D.C.] : Congressional Research Service, 2019- 2019

Programs affecting safety and innovation in pediatric therapies hearing before the Subcommittee on H

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2008. 2008

Trade and investment : mutual recognition : agreement between the United States of America and the E

[Washington, D.C.] : United States Department of State, [2017?] 2017

Annual report

Center for Devices and Radiological Health (U.S.). Office of Science and Technology.
Rockville, Md. : U.S. Food and Drug Administration, Center for Devices and Radiological Health 2001