CAMDR 2020 October 15-18 Edmonton, AB
Frequently asked questions regarding the revised CSA Z314-18
HEALTH CANADA NOTICE:
Classification and Licensing of High-Level Disinfectants and Sterilants as Medical Devices
In collaboration with Infection Prevention and Control Canada (IPAC), CAMDR has issued a comment on the Health Canada Notice: Classification and Licensing of High-Level Disinfectants and Sterilants as Medical Devices (March 16, 2018).
Notice: Classification and Licensing of High-Level Disinfectants and Sterilants as Medical Devices
CAN/CSA-Z314-18 – Canadian medical device reprocessing is now published and available on the CSA Store! http://shop.csa.ca/en/canada/sterilization/cancsa-z314-18/invt/27043922018
For information only: The FDA (US) has announced the release of the voluntary standardized protocols for duodenoscope sample collection and culture and a date for a webinar to go over the new protocol. This is a US protocol that provides guidance. Please click on the link to view. https://www.fda.gov/MedicalDevices/NewsEvents/WorkshopsConferences/ucm598194.htm
Education Modules – How to
Our Vision and Mission
Canadian Association of Medical Device Reprocessing (CAMDR) is a national voice and leader in Medical Device Reprocessing (MDR)practices. CAMDR collaborates with other national and international organizations to provide its members with professional development and to elevate the quality and standards.
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