In Person Medical Devices Training & Courses

Manufacturers of Class II, III and IV medical devices in Canada must establish and maintain a certified ISO 13485 Quality Management System in order to comply with Health Canada requirements and obtain and Medical Device Establishment License.

The BRC offers a full range of quality management training and related services for medical device manufacturers, suppliers and distributors.

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session

Delivery: In-Person

Available as a Dedicated Session