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20200315093000.0 |
| 008 |
170601s2017 ne eng |
| 020 |
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|a 9780081006252
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| 040 |
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|a UniSZA
|e rda
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| 050 |
0 |
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|a RM301.25
|b .M55 2017
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| 060 |
1 |
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|a QV 745
|b .M647 2017
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| 090 |
0 |
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|a RM301.25
|b .M55 2017
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| 100 |
1 |
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|a Miller, Susan ,
|d 1955- ,
|e author
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| 245 |
1 |
0 |
|a Managing the drug discovery process :
|b how to make it more efficient and cost effective
|c Susan M. Miller, Walter H. Moos, Barbara H. Munk, Stephen A. Munk
|
| 264 |
|
1 |
|a Amsterdam :
|b Elsevier/Woodhead Publishing
|c 2017
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| 300 |
|
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|a xxix, 506 pages :
|b illustration (some color) ;
|c 24 cm.
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| 336 |
|
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|a text
|2 rdacontent
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| 337 |
|
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|a unmediated
|2 rdamedia
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| 338 |
|
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|a volume
|2 rdacarrier
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| 504 |
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|a Includes bibliographical references and index
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| 505 |
0 |
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|a 1. Introduction and overview -- 2. Introduction: preprofessional education -- 3. Two-year certification and degree programs -- 4. Four-year undergraduate degree programs -- 5. The big decision -- 6. Graduate and postgraduate education at a crossroads -- 7. Master's degree programs -- 8. Doctoral and professional programs -- 9. The big leap -- 10. Drug discovery: Chaos can be your friend or your enemy -- 11. Drug discovery: Standing on the shoulders of giants -- 12. Research and discovery -- 13. Turning a potent agent into a registered product -- 14. Chemical development: Synthetic studies and engineering aspects -- 15. Chemical development: Analytical studies -- 16. FDA path and process: Sponsor`s regulatory tasks for drug approval -- 17. Epilogue
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| 650 |
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0 |
|a Cost-Benefit Analysis
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| 650 |
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0 |
|a Drug Discovery
|x Organization & administration
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| 650 |
|
0 |
|a Efficiency, Organizational
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| 700 |
1 |
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|a Moos, W. H. [
|q (Walter Hamilton)] ,
|d 1954- ,
|e editor
|
| 700 |
1 |
|
|a Munk, Barbara H. ,
|e editor
|
| 700 |
1 |
|
|a Munk, Stephen A. ,
|e editor
|
| 999 |
|
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|a 1000169244
|b Book
|c OPEN SHELF (30 DAYS)
|e Tembila Campus
|