WHO Expert Committee on Specifications for Pharmaceutical Preparations thirty-seventh report.
-д хадгалсан:
| Байгууллагын зохиогчид: | , |
|---|---|
| Формат: | Цахим Цахим ном |
| Хэл сонгох: | англи |
| Хэвлэсэн: |
Geneva :
World Health Organization,
2003.
|
| Цуврал: | Technical report series (World Health Organization) ;
908. |
| Нөхцлүүд: | |
| Онлайн хандалт: | An electronic book accessible through the World Wide Web; click to view |
| Шошгууд: |
Шошго нэмэх
Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!
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MARC
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| 110 | 2 | |a WHO Expert Committee on Specifications for Pharmaceutical Preparations. |b Meeting |n (37th : |d 2001 : |c Geneva, Switzerland) | |
| 245 | 1 | 0 | |a WHO Expert Committee on Specifications for Pharmaceutical Preparations |h [electronic resource] : |b thirty-seventh report. |
| 260 | |a Geneva : |b World Health Organization, |c 2003. | ||
| 300 | |a viii, 145 p. | ||
| 490 | 1 | |a WHO technical report series, |x 0512-3054 ; |v 908 | |
| 505 | 0 | |a 1. Introduction -- 2. General policy -- 3. Quality control--specifications and tests -- 4. Quality control--international reference materials -- 5. Quality control--national laboratories -- 6. Quality assurance--good manufacturing practices (GMP) -- 7. Quality assurance--inspection -- 8. Quality assurance--distribution and trade-related -- 9. Quality assurance--risk analysis -- 10. Quality assurance--drug supply -- 11. Quality assurance--storage -- 12. International Nonproprietary Names (INNs) Programme -- 13. Miscellaneous -- Annex 1. Recommendations on risk of transmitting animal spongiform encephalopathy agents via medicinal products -- Annex 2. The International Pharmacopoeia: revised concepts and future perspectives -- Annex 3. Guidelines on good manufacturing practices for radiopharmaceutical products -- Annex 4. Good manufacturing practices for pharmaceutial products: main prinicples -- Annex 5. Model certificate of good manufacturing practices -- Annex 6. Guidance on good manufacturing practices (GMP): inspection report -- Annex 7. Application of hazard analysis and critical control point (HACCP) method to pharmaceuticals -- Annex 8. Procedure for assessing the acceptability, in principle, of pharmaceutical products for purchase by United Nations agencies -- Annex 9. Guide to good storage practices for pharmaceuticals. | |
| 533 | |a Electronic reproduction. |b Palo Alto, Calif. : |c ebrary, |d 2009. |n Available via World Wide Web. |n Access may be limited to ebrary affiliated libraries. | ||
| 650 | 0 | |a Drugs |x Standards |v Congresses. | |
| 650 | 0 | |a Drugs |x Specifications |v Congresses. | |
| 650 | 0 | |a Pharmaceutical industry |x Quality control |v Congresses. | |
| 655 | 7 | |a Electronic books. |2 local | |
| 710 | 2 | |a ebrary, Inc. | |
| 830 | 0 | |a Technical report series (World Health Organization) ; |v 908. | |
| 856 | 4 | 0 | |u http://site.ebrary.com/lib/daystar/Doc?id=10040297 |z An electronic book accessible through the World Wide Web; click to view |
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