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Pharmaceutisch Weekblad

, Volume 2, Issue 1, pp 133–141 | Cite as

Enige ervaringen met de interpretatie van GMP-richtlijnen bij de bereiding en autoclavering van parenteralia

  • Ir. Th. M. Berg
Parenteralia

Samenvatting

Na een korte algemene inleidingover ‘Good Manufacturing Practice (gmp)’ worden enkele voorbeelden gegeven van interpretatie van GMP-richtlijnen in de farmaceutische industrie en wordt tenslotte een aanzet gegeven tot een discussie overgmp in de ziekenhuisapotheek.

Abstract

After a short general survey about ‘Good Manufacturing Practice (gmp)’ the interpretation of gmp rules in the pharmaceutical industry is illustrated by giving a few practical examples. Finally some thoughts are developed on how these rules can also be used in hospital pharmacy.

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Literatuur

  1. Fritzsche, U. (1978)Pharm. Ind. 40, 1036–1040.Google Scholar
  2. Guide to Good Pharmaceutical Manufacturing Practice (1977) Dept. of Health and Social Security, London, HMSO.Google Scholar
  3. Jordan, J. (1978)Pharm. Ind. 40, 776–777Google Scholar
  4. Juran, J.,Quality Control Handbook, McGraw-Hill Book Company, London.Google Scholar
  5. New Zealand Code of Good Practice for Manufacture and Distribution of Medicines (1978) Dept. of Health.Google Scholar
  6. Simmonds, M. (1978)Pharm. Ind. 40, 737–744.Google Scholar
  7. Susan, H. (1978)Int. Conference on GMPin the Pharmaceutical and related industries. Powder Advisory Centre, London.Google Scholar
  8. World Health Organ.Tech. Rept. Ser. 567 (1975) 25th Rep.Google Scholar
  9. World Health Organ.Exp. Comm. on specifications for pharmaceutical preparations, Geneva.Google Scholar

Copyright information

© Bohn, Scheltema & Holkema 1980

Authors and Affiliations

  • Ir. Th. M. Berg
    • 1
  1. 1.Organon International bvOss.

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