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Subject: "Product safety."
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Safety regulations

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Online Results (8)
1.
Premarket notification, 510(k) : regulatory requirements for medical devices
Published
Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health ; Washington, D.C. : For sale by the Supt. of Docs., U.S. G.P.O., [1990]
Online
Online book
Location
HathiTrust Digital Library >> Online Resource
Format
Books / Online
2.
Medical product regulation : drugs, biologics, and devices
Author
Dabrowska, Agata
Published
[Washington, D.C.] : Congressional Research Service, 2018-
Online
https://purl.fdlp.gov/GPO/gpo133583
Location
Yale Internet Resource >> None
Format
Online
3.
A delicate balance : FDA and the reform of the medical device approval process : hearing before the Special Committee on Aging, United States Senate, One Hundred Twelfth Congress, first session, Washington, DC, April 13, 2011
Author
United States. Congress. Senate. Special Committee on Aging
Published
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., U.S. G.P.O., 2011
Online
Online book
Location
HathiTrust Digital Library >> Online Resource
Format
Books / Online
4.
More information for better patient care : hearing of the Committee on Labor and Human Resources, United States Senate, One Hundred Fourth Congress, second session, on S. 1477, to amend the Federal Food, Drug, and Cosmetic Act and the Public Health Service Act to improve the regulation of food, drugs, devices, and biological products, February 22, 1996
Author
United States. Congress. Senate. Committee on Labor and Human Resources
Published
Washington : U.S. G.P.O. : For sale by the U.S. G.P.O., Supt. of Docs., Congressional Sales Office, 1996.
Online
Online book
4.L 11/4:S.HRG.104-445
Location
HathiTrust Digital Library >> Online Resource
Format
Books / Online
5.
A delicate balance FDA and the reform of the medical device approval process : hearing before the Special Committee on Aging, United States Senate, One Hundred Twelfth Congress, first session, Washington, DC, April 13, 2011
Author
United States. Congress. Senate. Special Committee on Aging
Published
Washington : U.S. G.P.O., 2011.
Online
http://purl.fdlp.gov/GPO/gpo13842
Location
Yale Internet Resource >> None
Format
Books / Online
6.
A delicate balance : FDA and the reform of the medical device approval process : hearing before the Special Committee on Aging, United States Senate, One Hundred Twelfth Congress, first session, Washington, DC, April 13, 2011
Author
United States. Congress. Senate. Special Committee on Aging
Published
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., U.S. G.P.O., 2011.
Location
Library Shelving Facility (LSF) >> Y 4.AG 4:S.HRG.112-92
Format
Books
7.
Revitalizing new product development from clinical trials through FDA review : hearing of the Committee on Labor and Human Resources, United States Senate, One Hundred Fourth Congress, second session, on S. 1477 ... February 21, 1996
Author
United States. Congress. Senate. Committee on Labor and Human Resources
Published
Washington : U.S. G.P.O. : For sale by the U.S. G.P.O., Supt. of Docs., Congressional Sales Office, 1996.
Online
Online book
Online book
4.L 11/4:S.HRG.104-444
Location
HathiTrust Digital Library >> Online Resource
Format
Books / Online
8.
Medical devices and the public's health the FDA 510(k) clearance process at 35 years
Author
Institute of Medicine (U.S.). Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process
Published
Washington, D.C. : National Academies Press, c2011.
Online
Online book
Location
Yale Internet Resource >> None
Format
Books / Online
9.
Medical device design and regulation
Author
DeMarco, Carl T.
Published
Milwaukee, Wisconsin : ASQ Quality Press, 2011.
Online
Online book
Location
Yale Internet Resource >> None
Format
Books / Online