PHL Series Steriele isolator voor cellulair etiketteren
Cellulair etiketteren bij nucleaire geneeskunde wordt geclassificeerd door goede radiopharmaceutische praktijknormen bij de voorbereiding van radiopharmaceutica in Nucleaire geneeskunde als “extempore preparaties” en deze moeten worden uitgevoerd in een kap met de laminaire stroming (klasse A) die zich bevindt in een omgeving klasse B, of binnen een isolator die de steriliteit kan handhaven en die zich bevindt in een omgeving klasse D.
Met de tweede oplossing wordt voorkomen dat een cleanroom moet worden opgesteld binnen de afdeling nucleaire geneeskunde en deze garandeert een volledige schepping van het product en de operator.
Het etiketteren wordt binnen de doos uitgevoerd, dankzij een paar handschoenen in de hoofdwand. Het materiaal gaat door de voorkamer (in klasse B) zodat de hoofdkamer nooit in rechtstreekse communicatie staat met de externe omgeving.
ISO 45001 Health and Safety Management System
ISO 14001 & ISO 50001 Environmental and energetic management system
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Radiofarmaceutisch
Pharma
ATMP Cel- en gentherapie
Services
