Road Show "EU Directive 2007/47/EC"
Regulatory framework of Medical Devices on its way into the futureSchedule: 10 am - 5 pmThe requirements of the New EU Directive 2007/47/EC will soon come into effect. From 21 March 2010 onward, the new provisions must be applied. We want you to be prepared!
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| Venue | Date | Language | Agenda | |
FIZ ConferenceLab  , Altenhöferallee 3, 60438 FRANKFURT | 30 Oct 2009 | English | Agenda | (Log in with password) |
| Medicallounge , Ohlauer Straße 43, 10999 BERLIN | 4 Nov 2009 | English | Agenda | (Log in with password) |
TÜV SÜD | 12 Nov 2009 | German | Agenda |
| Topics: | 1.) The most important changes by the New MDD 2.) Implementation into national laws (Germany, UK, France and Italy) 3.) Consequences and practical implementation from the view of a manufacturer 4.) Re-cast of the MDD – expectations for the future
Every presentation will be 30 minutes. Subsequent the participants have the opportunity of discussing their personal questions and of exchanging with experts and other participants. |
| Speaker: | Experts from the Federal Ministery of Health, the authority body and Medical device manufacturers will answer your personal questions and prepare you for the implementation.
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| Audience: | Managers, Quality and Regulatory Managers, Consultants
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Attendance fee: | € 200.- excl. or € 238.50 incl. VAT for non-customers € 150.- excl. or € 178.50 incl. VAT for customers The attendance fee includes refreshments and lunch.
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Registration: | Secure your place now! For a registration please fill in the After your registration you will receive a detailed agenda with more information on your chosen venue.
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| Organizer: | This Road Show is organized by TÜV SÜD Product Service GmbH.
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