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00000cam a2200000 7i4500 |
| 001 |
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20210317093000.0 |
| 008 |
170604s2017 flu eng |
| 020 |
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|a 9781482258905
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| 040 |
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|a UniSZA
|e rda
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| 050 |
0 |
0 |
|a RS192
|b .G66 2017
|
| 060 |
1 |
0 |
|a QV 778
|b .G646 2017
|
| 090 |
0 |
0 |
|a RS192
|b .G66 2017
|
| 245 |
0 |
0 |
|a Good design practices for GMP pharmaceutical facilities
|c edited byTerry Jacobs and Andrew A. Signore
|
| 250 |
|
|
|a 2nd ed
|
| 264 |
|
1 |
|a Boca Raton :
|b Taylor & Francis
|c 2017
|
| 300 |
|
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|a xvii, 516 pages :
|b illustration (some color) ;
|c 27 cm.
|
| 336 |
|
|
|a text
|2 rdacontent
|
| 337 |
|
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|a unmediated
|2 rdamedia
|
| 338 |
|
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|a volume
|2 rdacarrier
|
| 490 |
1 |
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|a Drugs and the pharmaceutical sciences
|
| 500 |
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|a Includes index
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| 505 |
0 |
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|a 1.Pharmaceutical industry profile -- 2. Current good manufacturing practices -- 3. Legacy facility master planning -- 4. Architectural design issues -- 5. Facility utility systems -- 6. High-purity water -- 7. Commissioning, qualification, and validation -- 8. Process engineering -- 9. Oral solid dosage facilities -- 10. Continuous oral solid dosage processing -- 11. Sterile manufacturing facilities -- 12. Biotechnology facilities -- 13. Codes and standards -- 14. Containment technology -- 15. Occupational health and safety -- 16. Sustainability -- 17. QA/QC laboratories and related support spaces -- 18. Packaging and warehousing
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| 650 |
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0 |
|a Drug factories
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| 650 |
|
0 |
|a Medical Pharmacology
|
| 650 |
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0 |
|a Pharmaceutical technology
|x Quality control
|
| 700 |
1 |
|
|a Jacobs, Terry ,
|e editor
|
| 700 |
1 |
|
|a Signore, Andrew A. ,
|e editor
|
| 999 |
|
|
|a 1000169302
|b Book
|c OPEN SHELF (30 DAYS)
|e Tembila Campus
|