Medical device safety : hearings before the Subcommittee on Health and the Environment of the Committee on Energy and Commerce, House of Representatives, One Hundred First Congress on H.R. 3095 ... November 6, 1989 and July 17, 1990
Saved in:
Corporate Author: | United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health and the Environment |
---|---|
Format: | Book |
Language: | English |
Published: |
Washington :
U.S. G.P.O.,
1990
|
Subjects: | |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Medical device safety : hearings before the Subcommittee on Health and the Environment of the Committee on Energy and Commerce, House of Representatives, One Hundred First Congress on H.R. 3095, a bill to amend the Federal Food, Drug, and Cosmetic Act to make improvements in the regulation of medical devices, and for other purposes, November 6, 1989 and July 17, 1990.
Published: (1990) -
Approval of medical devices : European Union, Australia, Brazil, Canada, China, France, Germany, Israel, Japan, Mexico, Netherlands, Russian Federation, South Africa, Spain, Switzerland, United Kingdom.
Published: (2014) -
Medical devices : are current regulations doing enough for patients? : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Eleventh Congress, first session, June 18, 2009
Published: (2012) -
Medical devices : are current regulations doing enough for patients? : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Eleventh Congress, first session, June 18, 2009.
Published: (2012) -
Medical devices : hearings before the Subcommittee on Public Health and Environment of the Committee on Interstate and Foreign Commerce, House of Representatives, Ninety-third Congress, first session on H.R. 6073 and H.R. 9984, bills to protect the public health by amending the Federal Food, Drug, and Cosmetic Act to assure the safety and effectiveness of medical devices : H.R. 539, a bill to create a national commission to study quality controls and manufacturing procedures of medical devices, surgical instruments, artificial organs and limbs, therapeutic instruments and devices, and other medical and hospital equipment, and for other purposes : H.R. 10061, a bill to regulate defective, ineffective, and unreliable medical devices, October 23 and 24, 1973.
Published: (1974)