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Samenvatting het geneesmiddel H5

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Samenvatting van 1 pagina's voor het vak Het Geneesmiddel aan de KU Leuven (Samenvatting H5)

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Uploaded on
December 30, 2022
Number of pages
1
Written in
2020/2021
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Summary

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H5: analyse en kwaliteitscontrole
1 HARMONISATIE VAN DE KWALITEITSNORMEN VOOR
FARMACEUTISCHE GRONDSTOFFEN OP EUROPEES NIVEAU
Tot 1960: ieder land een eigen farmacopee (wetboek van de farmaceutische industrie en de apotheker)
 kwaliteitsnormen en lijst opgenomen grondstoffen niet uniform

1964: 8 landen van raad van Europa beslissen hun nationale farmacopees te harmoniseren  oprichting
Europese Farmacopeecommissie

Harmonisatie  vergemakkelijking verkoop en zelfde normen maken geneesmiddelen veiliger (geen
angst dat geneesmiddel niet aan normen van eigen land voldoet)

1969: uitgave 1e Europese Farmacopee  meer en meer landen nemen deel  heden: 39 Europese
landen

2 delen EF:

 Algemeen deel
o General notices
o Analysetechnieken
o Te gebruiken recipiënten
o Te gebruiken reagentia

 Monografieën: teksten die de normen beschrijven in verband met zuiverheid en gehalte van een
farmaceutische grondstof
o Enkelvoudige stoffen: actieve stoffen en hulpstoffen
o Toedieningsvormen



De farmacopee wordt regelmatig aangepast (België om de 30 jaar) door nieuwe verworven kennis.
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