This webinar will include a comprehensive overview of the regulatory approval process in the European Union for medical devices. The webinar will also cover the registration process from CE Marking to market access for medical devices, equipment, instruments and disposables as well as dental equipment and supplies. Marc-Henri Winter, Technical Director of LNE-GMED, will share his experience in processing EU registration for American companies. Marjorie Cote, QA/QR Director of Pulpdent, will present on her experience as a small American company entering the EU market. Diagnostics and pharmaceuticals will not be included in this overview.
Details
Date: Tuesday, February 9, 2010
Time: Noon to 1 p.m. ET
Location: Your computer
Fee: $95 per participant
Webinar Overview
- How do I register my product in the EU?
- Can my in-country distributor help with the regulatory approval process?
- Does it matter which country is approached first for classification?
- What are other companies doing to be successful in these markets?
- How much does it cost?
Presenters
Marc-Henri Winter, Technical Director, LNE-GMED1
Biography2
Testimonial: Marjorie Cote, QA/RA Director, Pulpdent
Registration
To register for either event, please visit: http://www.buyusa.gov/healthcare/eu_registration.html
Contact Information
If you have any questions, please contact Julia Zorzi via email at Julia.Zorzi@mail.doc.gov or by phone at 412-644-2800.