Description:

A timely, fast and successful application process is the beginning of many product success stories in Canada.  Module II(a) covers:

• Application Requirements for Medical Devices Class III & IV, Non-IVDD
• Scientific Screening and Common Deficiencies for Medical Devices Class III & IV, Non-IVDD 

Module II(b) covers:

• Scientific Review, Quality Issues and Common Additional Information Requests for Medical Devices Class III & IV

Each webcast is approximately 1.5 hours in length.

Speakers:

All presenters are from Health Canada's Medical Devices Bureau.

Module II(a) speaker is Constance Campbell, Device Evaluation Division

Who should attend?

• Regulatory Affairs Associates of all levels
• Quality Assurance Managers / Associates
• Research & Development Managers/ Associates

Registration Information:

MEDEC Members:  $50 plus tax

Non-Members:  $75 plus tax

NOTE:  It will be about 24 hours from the time you register to the time you receive the connection information.

Cancellation Policy: Cancellations must be received in writing 10 business days prior to the date of the webcast to qualify for a refund. Substitutions are permitted. Failure to show will result in full fee charge. Payment must be received prior to the start of the webcast. Registrations become effective only when payment has been received by MEDEC.