Transcription of MODEL STANDARDS FOR PHARMACY COMPOUNDING OF
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MODEL STANDARDS FOR PHARMACY COMPOUNDING OF
MODEL STANDARDS FOR PHARMACY COMPOUNDING OFHAZARDOUSSTERILE PREPARATIONS MODEL STANDARDS for PHARMACY COMPOUNDING of Hazardous Sterile PreparationsApproved by the National Association of PHARMACY Regulatory Authorities (NAPRA) Board of Directors April 2015, published September November 2016 (Sterilization by Filtration in the Glossary corrected to 30 psi from 50 psi previously published).Adapted with permission from Pr paration de produits st riles dangereux en pharmacie Norme , Ordre des pharmaciens du Qu bec, 2014. National Association of PHARMACY Regulatory Authorities, 2016. All rights part of this document may be reproduced in any form by any photographic, electronic, mechanical or other means, or used in any information storage and retrieval system, without the written permission of the National Association of PHARMACY Regulatory Authorities (NAPRA) 130 Albert Street, Suite 1800, Ottawa, ON K1P 5G4 E-mail: | Telephone: (613) 569-9658 | Fax (613) 569-9659 ACKNOWLEDGEMENTS The National Association of PHARMACY Regulatory Authorities (NAPRA) would like to first thank one of its members, the Ordre des pharmaciens du Qu bec, for having made possible the adaptation of its document entitled Pr paration de produits st riles dangereux en pharmacie Norme to create this national document, MODEL STANDARDS for PHARMACY COMPOUNDING of Hazardous Sterile Preparations.
The preparation of medications (pharmacy compounding) has always been an integral part of the practice of pharmacy. It is essential to the delivery of health care and allows for personalized therapeutic solutions to improve patient care. However, pharmacy compounding must always be carried out within a prescriber–patient–pharmacist ...
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