How to Obtain a Canadian Medical Device License

 January 7, 2013


Online Event
2600 E.Bayshore Road
Palo Alto, California 94303


This webinar will help you understand the process for obtaining a Canadian Medical Device License. You will learn best practices for determining which device classification is appropriate for your device, which guidance documents you will need, best practices in preparing regulatory submissions for Class 3 and 4 products, which labeling changes your company needs to make, and the most effective approach for responding to requests for additional information.

Why Should You Attend:

Canada is usually the best market to target for a new medical product introduction. There are four reasons for this. First, the users are similar to the larger markets of the US and Europe. Second, the Canada regulations are simpler to learn. Third, the process for obtaining a medical device license is less burdensome than the 510(k) process in the USA and the CE Marking process in Europe. Fourth, the Canadian market is an ideal size for a pilot commercial product launch.

This webinar will provide valuable assistance to all medical device companies in preparing a Canadian Medical Device License Application. The focus will be upon creating an outline of the tasks that need to be completed ? without confusing everyone with regulatory jargon. This is a prerequisite for any company that wants to sell a Class 2, 3 or 4 medical device in Canada.

Organized by

2600 E. Bayshore Road
Palo Alto, California 94303
United States of America

More Information

Contact: Referral
Phone: +1-650-620-3915

Event's Website

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