The Library of Congress > Linked Data Service
  Label Dataset Type Subdivision Identifier
1. United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions. FDA's drug approval process Washington: U.S. G.P.O. For sale by the Supt. of Docs., U.S. G.P.O.; 2005

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Instance 14184419
2. United States. Congress. House. Committee on Government Reform and Oversight. Subcommittee on National Economic Growth, Natural Resources, and Regulatory Affairs. FDA medical product approvals Washington: U.S. G.P.O. For sale by the U.S. G.P.O., Supt. of Docs., Congressional Sales Office; 1997

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Instance 3551468
3. United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations. FDA's generic drug enforcement and approval process Washington: U.S. G.P.O. For sale by the U.S. G.P.O., Supt. of Docs., Congressional Sales Office; 1992

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Instance 1568393
4. United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations. FDA's generic drug approval process Washington: U.S. G.P.O. For sale by the Supt. of Docs., Congressional Sales Office, U.S. G.P.O.; 1989-1991

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5. United States. Congress. House. Committee on Government Operations. Intergovernmental Relations and Human Resources Subcommittee. FDA's approval of the Today contraceptive sponge Washington: U.S. G.P.O.; 1984

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6. United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations. FDA's generic drug approval process

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3883056
7. United States. Congress. House. Committee on Government Operations. Intergovernmental Relations and Human Resources Subcommittee. FDA's approval of the Today contraceptive sponge

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4782175
8. United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions. FDA's drug approval process

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Text
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14184419
9. United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations. FDA's generic drug enforcement and approval process

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Text
Monograph
1568393
10. United States. Congress. House. Committee on Government Reform and Oversight. Subcommittee on National Economic Growth, Natural Resources, and Regulatory Affairs. FDA medical product approvals

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3551468
11. Sasinowski, Frank J. Drug and biologic approvals Washington, DC: FDLI; c2000

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12. Premarket approval manual

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13. Market Intelligence Research Corporation Therapeutic and surgical equipment markets Mountain View, CA: Market Intelligence; c1993

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14. HIMA Educational Seminar on "FDA's Final Rule on Premarket Approval of Medical Devices and Diagnostic Products" (1986 : Washington, D.C.)

LC Name Authority File (LCNAF)
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n88034024
Educational Seminar on "FDA's Final Rule on Premarket Approval of Medical Devices and Diagnostic Products," HIMA ; Seminar on "FDA's Final Rule on Premarket Approval of Medical Devices and Diagnostic Products," HIMA Educational


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