Description:

This workshop is designed to provide medical device companies with an overview of the European Union (EU) regulatory system. You will gain the know-how to systematically seek regulatory approval for your medical devices. The workshop will prepare you for exporting your product to the EU market.

Calgary Location:  G382, AstraZeneca Videoconference Room, Heritage Medical Research Building, Foothills Campus, University of Calgary.  Click here for a map.  Park in Lot #6 - click here for map.

Edmonton Location:  Alberta Room, Commerce Place, 12th Floor, 10155 - 102 Street, Edmonton.

Speakers:

Manuela Ahlers, an expert with TÜV NORD CERT GmbH

Who should attend?

• Regulatory Affairs associates of all levels

Registration Information:

Regular (non-members): $75 plus taxes

MEDEC and Clinexus Members:  $55 plus taxes 

Cancellation Policy:  Cancellations must be received in writing by September 2, 2011 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 conference.  Registrations become effective only when payment has been received by MEDEC.

Thanks to our partners