Canadian medical device reprocessing
1.1
This Standard is intended to address the safe, effective, and reliable reprocessing of reusable medical
devices at each phase of the reprocessing workflow, including
a) establishing a QMS for the MDRD, including
i) key performance indicators;
ii) policies and procedures;
iii) documentation;
iv) roles and responsibilities;
v) management review;
vi) planning, resources and operations…
