CE Workshop for Medical Devices: How to successfully gain access to the EU Market
September 13, 2010
Presented by:
Overview
This workshop is designed to provide medical device companies with an overview of the European Union (EU) regulatory system. Manuela Ahlers, an expert with TUV NORD CERT GmbH has been invited to give you the know-how to systematically seek regulatory approval for your medical devices.
This workshop will prepare you for exporting your product to the EU market and will be an interactive full day workshop.
View Agenda
Topics
- Overall description of the European "Global Approach"
- Description of the different conformity assessment procedures (Modular System)
- Special Requirements of Medical Devices Directive
- Outsourcing of processes; subcontracting; OEM/Private labeling
- Case Studies/Workshop
Details
Date: Monday, September 13, 2010
Time: 8:30 am - 5:00 pm (registration and breakfast at 8:00 am)
Location: Strategy Room 320 - Morris J. Wosk Centre for Dialogue, 580 West Hastings Street (enter via Seymour Street courtyard entrance)
Registration
LifeSciences BC & MEDEC Members - $95.00 plus tax
Non-members - $105.00 plus tax
Click here to register
Join us after the workshop for our Medical Device Mingler. This networking reception provides an opportunity for members of the medical device community to meet and network in a casual setting.
Follow this link for more information and registration: http://mingler.eventbrite.com
