| Tag |
First Indicator |
Second Indicator |
Subfields |
| LEADER |
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| 001 |
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20191203131201.0 |
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|a QV 771
|b N5318 2004
|
| 245 |
0 |
0 |
|a New drug approval process :
|b accelerating global registrations /
|c edited by Richard A. Guarino.
|
| 250 |
|
|
|a Fourth edition.
|
| 264 |
|
1 |
|a New York :
|b M. Dekker,
|c [2004]
|
| 264 |
|
4 |
|c ©2004
|
| 300 |
|
|
|a xiv, 635 pages :
|b illustrations ;
|c 24 cm.
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| 336 |
|
|
|a text
|2 rdacontent
|b txt
|
| 337 |
|
|
|a unmediated
|2 rdamedia
|
| 338 |
|
|
|a volume
|2 rdacarrier
|b nc
|
| 490 |
1 |
|
|a Drugs and the pharmaceutical sciences ;
|v v.139
|
| 504 |
|
|
|a Includes bibliographical references and index.
|
| 505 |
0 |
|
|a pt. I. Regulatory practices and procedures of new drug, biologic, and device development -- pt. II. Clinical research development -- pt. III. Specific aspects in the process of new product submissions -- pt. IV. Global applications of good clinical practices (GCPs) -- pt. V. Effective and new methodologies in expediting new product approvals in the U.S. and European Union
|
| 650 |
|
2 |
|a Drug Approval.
|
| 650 |
|
2 |
|a Clinical Trials as Topic
|x standards
|z United States.
|
| 650 |
|
2 |
|a Drug Evaluation
|x standards
|z United States.
|
| 700 |
1 |
|
|a Guarino, Richard A.,
|d 1935-
|
| 830 |
|
0 |
|a Drugs and the pharmaceutical sciences ;
|v v.139.
|
| 948 |
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|
|a AE : QV 771 N5318 1987, 1993, 2000
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| 948 |
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|a 5th ed. not purchased; 2/0 use on this; 9/16/09, ngb
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|a Texas A&M University
|b Rellis Campus
|c Joint Library Facility
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|i unmediated -- volume
|m 323890186365B
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