When: Tuesday, February 9, 2010 - 12:00pm-1:00pm ET
Cost: $95 per person
Join the U.S. Commercial Service for a comprehensive review of the regulatory approval process in the European Union for medical devices.
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?
Scope
Registration process from CE Marking to market access for the following:
- Medical Devices
- Medical Equipment
- Instruments and Disposables
- Dental equipment and supplies
- * Diagnostics and pharmaceuticals will not be included in this overview
Presenters
Marc-Henri Winter, title of LNE-GMED (http://www.lne-gmed.com/), will share his experience in processing EU registration for American companies.
Marjorie Cote, QA/RA Director of Pulpdent (http://www.pulpdent.com/) will present on her experience as a small American company entering the EU market.
Registration
Registration is available online by clicking here!
Inquiries
If you have questions, please contact:
|
Ms. Pompeya Lambrecht Email: Pompeya.Lambrecht@mail.doc.gov Phone: 602.277.5223 |
Ms. Rochelle Williams Email: Rochelle.Williams@mail.doc.gov Phone: 619.557.5899 |