Canadian medical device reprocessing in all health care settings
1 Scope
1.1 Standard addresses
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 MDRA, including
i) key performance indicators;
ii) policies and procedures;
iii) documentation;
iv) roles and responsibilities;
v) management review;
vi) planning…
Purpose
1.1 Purpose
This Standard specifies technical requirements on how to make buildings and the exterior built environment accessible and safely usable by persons with physical, sensory, or cognitive disabilities.
Notes:
1) Temporary buildings and facilities provided for public use should also comply with the technical requirements of this Standard. Such temporary facilities can…
This Standard specifies minimum requirements for zero-copy integration and includes a set of guidelines
for building modular capabilities within a controlled data management environment which can be
applied either as stand-alone experiences or combined into advanced solutions.
This Standard provides a blueprint for IT and other leaders who rely on organizational data integrity to
perform…
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