Oct 31, 2013
Medical device market regulators in Canada have added 11 new items to their list of recognized standards, removed six and amended another 27.
Standards newly recognized by Health Canada include IEC and ISO standards covering various electrical medical device components, implantable devices and IVDs.
Standards deleted from Health Canada’s list include three IEC electromagnetic compatibility standards, two ASTM standards covering steel and metal device materials, and one ISO standard for ceramic implant materials.
Companies holding Medical Device Licenses or Medical Device Establishment Licenses for medical devices, or firms planning to apply for Canadian market authorization, should make sure their compliance with pertinent standards is up to date.
Canadian medical device market regulator Health Canada plans to issue only electronic versions of new and amended Medical Device Establishment Licenses (MDEL) and Medical Device Licenses (MDL) starting November 1, 2013.
According to an email from Health Canada's Medical Devices Bureau, no more hard copies of new or amended licenses will be sent out to medical device manufacturers in order to boost process efficiencies at the regulator.
Applicants for medical device licensing in Canada should be sure to include appropriate email addresses in their submissions in order to properly receive registration documents. Questions regarding this new policy can be sent to mdb_enquiries@hc-sc.gc.ca.
Health Canada has announced changes to its list of recognized list of medical device