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WHO Expert Committee on Specifications for Pharmaceutical Preparations - [electronic resource] : thirty-seventh report.
WHO Expert Committee on Specifications for Pharmaceutical Preparations - [electronic resource] : thirty-seventh report.
Detailed Information
- 자료유형
- 비도서
- ISBN
- 0585492719 (electronic bk.)
- 미국회청구기호
- RS189-.W49 2003eb
- DDC
- 615.1-22
- 회의명
- WHO Expert Committee on Specifications for Pharmaceutical Preparations. (37th, 2001 . Geneva, Switzerland)
- 서명/저자
- WHO Expert Committee on Specifications for Pharmaceutical Preparations - [electronic resource] : thirty-seventh report.
- 발행사항
- Geneva : World Health Organization, 2003.
- 형태사항
- viii, 136 p. ; 24 cm.
- 총서명
- WHO technical report series = 0512-3054 ; 908
- 내용주기
- 완전내용1. Introduction -- 2. General policy -- 3. Quality control--specifications andtests -- 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. Recommendationson risk of transmitting animal spongiform encephalopathy agents via medicinal products -- Annex 2. The International Pharmacopoeia: revised concepts and futureperspectives -- Annex 3. Guidelines on good manufacturing practices for radiopharmaceutical products -- Annex 4. Good manufacturing practices for pharmaceutialproducts: main prinicples -- Annex 5. Model certificate of good manufacturing practices -- Annex 6. Guidance on good manufacturing practice
- 복제주기
- Electronic reproduction. . Boulder, Colo. : NetLibrary, 2004. Available via World Wide Web. Access may be limited to NetLibrary affiliated libraries.
- 일반주제명
- Drugs Specifications Congresses. Drugs Standards Congresses. Pharmaceutical industry Quality control Congresses. Chemistry, Pharmaceutical Congresses. Pharmaceutical Preparations standards Congresses. Drugs, Generic standards Congresses. Pharmacopoeias Congresses. Prion Diseases transmission. Quality Control Congresses. Reference Standards Congresses.
- 기타저자
- NetLibrary, Inc.
- 기타형태저록
- . Original. 9241209089. (OCoLC)52225572
- 통일총서명
- Technical report series (World Health Organization) ; 908.
- 전자적 위치 및 접속
- Technical report series (World Health Organization) ; 908.
- Control Number
- gtec:53231
MARC
008040129s2003 sz s i100 0 eng d■003 OCoLC
■020 ▼a0585492719 (electronic bk.)
■040 ▼aN▼T▼cN▼T▼dOCLCQ
■05014▼aRS189▼b.W49 2003eb
■0701 ▼a449.9▼bW892T no. 908
■08204▼a615.1▼222
■090 ▼a ▼b
■1112 ▼aWHO Expert Committee on Specifications for Pharmaceutical Preparations▼n(37th▼d2001 ▼cGeneva, Switzerland)
■24510▼aWHO Expert Committee on Specifications for Pharmaceutical Preparations▼h[electronic resource] ▼bthirty-seventh report.
■260 ▼aGeneva ▼bWorld Health Organization▼c2003.
■300 ▼aviii, 136 p. ▼c24 cm.
■4901 ▼aWHO technical report series▼x0512-3054 ▼v908
■5050 ▼a1. Introduction -- 2. General policy -- 3. Quality control--specifications andtests -- 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. Recommendationson risk of transmitting animal spongiform encephalopathy agents via medicinal products -- Annex 2. The International Pharmacopoeia: revised concepts and futureperspectives -- Annex 3. Guidelines on good manufacturing practices for radiopharmaceutical products -- Annex 4. Good manufacturing practices for pharmaceutialproducts: main prinicples -- Annex 5. Model certificate of good manufacturing practices -- Annex 6. Guidance on good manufacturing practice
■533 ▼aElectronic reproduction.▼bBoulder, Colo. ▼cNetLibrary▼d2004.▼nAvailable via World Wide Web.▼nAccess may be limited to NetLibrary affiliated libraries.
■6500 ▼aDrugs▼xSpecifications▼vCongresses.▼aDrugs▼xStandards▼vCongresses.▼aPharmaceutical industry▼xQuality control▼vCongresses.▼aChemistry, Pharmaceutical▼vCongresses.▼aPharmaceutical Preparations▼xstandards▼vCongresses.▼aDrugs, Generic▼xstandards▼vCongresses.▼aPharmacopoeias▼vCongresses.▼aPrion Diseases▼xtransmission.▼aQuality Control▼vCongresses.▼aReference Standards▼vCongresses.
■6557 ▼aElectronic books.▼2local
■7102 ▼aNetLibrary, Inc.▼aWorld Health Organization.
■7761 ▼cOriginal▼z9241209089▼w(OCoLC)52225572
■8300 ▼aTechnical report series (World Health Organization) ▼v908.
■8564 ▼3Bibliographic record display▼uhttp://www.netLibrary.com/urlapi.asp?action=summary&v=1&bookid=102431▼zAn electronic book accessible through the World Wide Web;click for information
■994 ▼a92▼bAMF
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