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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 resou...
WHO Expert Committee on Specifications for Pharmaceutical Preparations - [electronic resource] : thirty-seventh report.

상세정보

자료유형  
 비도서
ISBN  
0585492719 (electronic bk.)
미국회청구기호  
RS189-.W49 2003eb
DDC  
615.1-22
청구기호  
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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