With more than 1000 medical device manufacturing facilities and a strong presence in the medical device market with about 60% of their imports coming from the United States and other regions of the world, all medical devices sold into the Canadian market must comply with Canadian medical device regulations.

E & E Medicals and consulting helps its clients understand and comply with Canada medical device regulations. We will work closely with you to determine how your device is classified and prepare the necessary documentation to meet Canadian medical device regulations.

To learn more about our Canadian licence applications contact us today