WHO Expert Committee on Specifications for Pharmaceutical Preparations : thirty-seventh report.

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Bibliographic Details
Superior document:WHO technical report series, 908
:
TeilnehmendeR:
Year of Publication:2003
Language:English
Series:Technical report series (World Health Organization) ; 908.
Online Access:
Physical Description:viii, 145 p.
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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. Ann Arbor, MI : ProQuest, 2015. Available via World Wide Web. Access may be limited to ProQuest 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 4 |a Electronic books. 
710 2 |a ProQuest (Firm) 
830 0 |a Technical report series (World Health Organization) ;  |v 908. 
856 4 0 |u https://ebookcentral.proquest.com/lib/oeawat/detail.action?docID=284793  |z Click to View