Date: Tuesday, February 9, 2010
Time: noon ET * 11 a.m. CT * 9 a.m. PT
Duration: 1 Hour

Fee: $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.   Marc-Henri Winter, title of LNE-GMED, will share his experience in processing EU registration for American companies. 

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 medical devices, medical equipment, instruments and disposables as well as dental equipment and supplies will be addressed.  Diagnostics and pharmaceuticals will not be included in this overview.

Presenter
Marc-Henri Winter, Technical Director, LNE-GMED
Biography

Registration
To register, please click link below
https://emenuapps.ita.doc.gov/ePublic/newWebinarRegistration.jsp?SmartCode=0Q2A

Inquiries
For direct e-mail inquiries, please contact Pompeya Lambrecht at pompeya.lambrecht@N0SPAM.N0SPAM.mail.doc.gov or rochelle.williams@N0SPAM.NOSPAM.mail.doc.gov  
Via phone, Pompeya can be reached at 602.277.5223 and Rochelle at 619.557.5899.

To download Medical Device Registration in the EU Flyer, please click here