MEDEC and the Medical Devices Bureau (MDB) of Health Canada are pleased to offer webcasts on all pre-market activities and the latest developments and requirements on Health Canada submissions for a Canadian license under the Canadian Medical Devices Regulations.  If a timely, fast and successful application is important to your business, you will not want to miss this series of webcasts that will introduce and update participants on:

• Requirements for a Canadian license
• Use of STED documents
• Scientific screening and common deficiencies
• Scientific review and additional information requests
• Amendments and significant changes

Note:  These are the archives of the live webcasts held in 2010.

Click here to view the webcast brochure.  All webcasts are approximately 1.5 hours long.

Speakers

All presenters are from Health Canada's Medical Devices Bureau

Who should attend?

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

Registration Information

MEDEC members:  $50 plus tax per module session

Non-MEDEC members:  $75 plus tax per module session

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

For more information and to register:

• Module I (a) and (b) - Click here to register to view the archived webcast.
• Module II (a) and (b) (non-IVD) - Click here to register to view the archived webcast.
• Module III (IVDD) - Click here to register to view the archived webcast.
• Module IV - Click here to register to view the archived webcast.

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.