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|a EEXU
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|a 1020-C (online)
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|a Y 4.J 89/1:115-27
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| 088 |
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|a Serial no. 115-27 (United States. Congress. House. Committee on the Judiciary)
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| 099 |
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|a Y 4.J 89/1:115-27 Online
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| 110 |
1 |
|
|a United States.
|b Congress.
|b House.
|b Committee on the Judiciary.
|b Subcommittee on Regulatory Reform, Commercial and Antitrust Law,
|e author.
|0 http://id.loc.gov/authorities/names/no2013088204
|
| 245 |
1 |
0 |
|a Antitrust concerns and the FDA approval process :
|b hearing before the Subcommittee on Regulatory Reform, Commercial and Antitrust Law of the Committee on the Judiciary, House of Representatives, One Hundred Fifteenth Congress, first session, July 27, 2017.
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| 246 |
3 |
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|a Antitrust concerns and the Food and Drug Administration approval process
|
| 264 |
|
1 |
|a Washington :
|b U.S. Government Publishing Office,
|c 2018.
|
| 300 |
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|a 1 online resource (iv, 51 pages)
|
| 336 |
|
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|a text
|b txt
|2 rdacontent
|
| 337 |
|
|
|a computer
|b c
|2 rdamedia
|
| 338 |
|
|
|a online resource
|b cr
|2 rdacarrier
|
| 500 |
|
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|a "Serial number 115-27."
|
| 588 |
0 |
|
|a Online resource; title from PDF title screens (govinfo web site, viewed on June 27, 2018).
|
| 610 |
1 |
0 |
|a United States.
|b Food and Drug Administration
|v Rules and practice.
|0 http://id.loc.gov/authorities/names/n80126147
|
| 650 |
|
0 |
|a Drugs
|z United States
|x Testing.
|0 http://id.loc.gov/authorities/subjects/sh2009123883
|
| 650 |
|
0 |
|a Drug approval
|z United States.
|0 http://id.loc.gov/authorities/subjects/sh2009123884
|
| 650 |
|
0 |
|a Drugs
|x Safety regulations
|z United States.
|0 http://id.loc.gov/authorities/subjects/sh85039719
|
| 650 |
|
0 |
|a Medical instruments and apparatus
|x Safety regulations
|z United States.
|0 http://id.loc.gov/authorities/subjects/sh2008107639
|
| 650 |
|
0 |
|a Generic drugs
|z United States.
|0 http://id.loc.gov/authorities/subjects/sh2009125738
|
| 650 |
|
0 |
|a Competition
|z United States.
|0 http://id.loc.gov/authorities/subjects/sh2008100014
|
| 650 |
|
0 |
|a Antitrust law
|z United States.
|0 http://id.loc.gov/authorities/subjects/sh2007100529
|
| 610 |
1 |
7 |
|a United States.
|b Food and Drug Administration.
|2 fast
|0 (OCoLC)fst00549734
|
| 650 |
|
7 |
|a Antitrust law.
|2 fast
|0 (OCoLC)fst00810849
|
| 650 |
|
7 |
|a Competition.
|2 fast
|0 (OCoLC)fst00871464
|
| 650 |
|
7 |
|a Drug approval.
|2 fast
|0 (OCoLC)fst00898661
|
| 650 |
|
7 |
|a Drugs
|x Safety regulations.
|2 fast
|0 (OCoLC)fst00898910
|
| 650 |
|
7 |
|a Drugs
|x Testing.
|2 fast
|0 (OCoLC)fst00898940
|
| 650 |
|
7 |
|a Generic drugs.
|2 fast
|0 (OCoLC)fst00939969
|
| 650 |
|
7 |
|a Medical instruments and apparatus
|x Safety regulations.
|2 fast
|0 (OCoLC)fst01014229
|
| 651 |
|
7 |
|a United States.
|2 fast
|0 (OCoLC)fst01204155
|
| 776 |
0 |
8 |
|i Print version:
|a United States. Congress. House. Committee on the Judiciary. Subcommittee on Regulatory Reform, Commercial and Antitrust Law.
|t Antitrust concerns and the FDA approval process
|w (OCoLC)1042073889
|
| 776 |
0 |
8 |
|i Microfiche version:
|a United States. Congress. House. Committee on the Judiciary. Subcommittee on Regulatory Reform, Commercial and Antitrust Law.
|t Antitrust concerns and the FDA approval process
|w (OCoLC)1078924440
|
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|u https://purl.fdlp.gov/GPO/gpo93483
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|a Michigan State University-Library of Michigan
|b Michigan State University
|c MSU Online Resource
|d MSU Government Documents Online Resource
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|e Y 4.J 89/1:115-27 Online
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|i Electronic Resource
|n 1
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