LDR | |
01912cam a2200421 a 4500 |
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011339075 |
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MiAaHDL |
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20110215000000.0 |
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m d |
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cr bn ---auaua |
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830906s1982 dcua b f000 0 eng c |
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019 |
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035 |
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035 |
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035 |
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040 |
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‡aDGPO/DLC
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043 |
⊔ |
⊔ |
‡an-us---
|
049 |
⊔ |
⊔ |
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050 |
0 |
0 |
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060 |
0 |
0 |
‡aQV 771
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082 |
0 |
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‡219
|
086 |
0 |
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‡aY 4.G 74/7:D 84/14
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110 |
1 |
⊔ |
‡aUnited States.
‡bCongress.
‡bHouse.
‡bCommittee on Government Operations.
‡bIntergovernmental Relations and Human Resources Subcommittee.
|
245 |
1 |
4 |
‡aThe regulation of new drugs by the Food and Drug Administration :
‡bthe new drug review process : hearings before a subcommittee of the Committee on Government Operations, House of Representatives, Ninety-seventh Congress, second session, August 3 and 4, 1982.
|
260 |
⊔ |
⊔ |
‡aWashington :
‡bU.S. G.P.O. :
‡b[For sale by the Supt. of Docs., U.S. G.P.O., Congressional Sales Office],
‡c1982.
|
300 |
⊔ |
⊔ |
‡avii, 688 p. :
‡bill. ;
‡c24 cm.
|
500 |
⊔ |
⊔ |
‡aItem 1016-A, 1016-B (microfiche).
|
504 |
⊔ |
⊔ |
‡aIncludes bibliographical references.
|
538 |
⊔ |
⊔ |
‡aMode of access: Internet.
|
610 |
1 |
2 |
‡aUnited States.
‡bFood and Drug Administration.
|
610 |
1 |
0 |
‡aUnited States.
‡bFood and Drug Administration.
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650 |
⊔ |
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‡aLegislation, Drug
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650 |
⊔ |
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‡aDrug Evaluation, Preclinical
‡zUnited States
‡vLegislation.
|
650 |
⊔ |
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‡aDrug Evaluation
‡zUnited States
‡vLegislation.
|
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⊔ |
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‡aClinical Trials
‡zUnited States
‡vLegislation.
|
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⊔ |
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‡aDrugs
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‡xTesting.
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‡aPharmacy
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‡zUnited States.
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⊔ |
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‡aDrugs
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|
740 |
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‡aNew drug review process.
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CID |
⊔ |
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‡a011339075
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DAT |
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DAT |
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‡a20120815064345.0
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CAT |
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‡aSDR-PUR
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FMT |
⊔ |
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‡aBK
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HOL |
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974 |
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