Hear the most recent practical experience with the 2007/47/EC Directive and find out the best new ways to improve PMS and Vigilance methods for your products under the new system
Informa Life Sciences annual
Medical Device Post Market Surveillance and Vigilance 2011 conference is now in its 6
th successful year. This year will now deliver recent case studies from Industry on how the March 2010 Medical Device Directive has been implemented. This conference allows you to hear from Member States and Notified bodies from a variety of different countries to hear new requirements and provide solutions. Also hear up-to-date information about new electronic vigilance systems that can make reporting for your Industry much easier.
2011 Conference Highlights
- Member States AND Notified Bodies discuss PMS and Vigilance requirement updates
- Hear practical Industry case studies on their experience and implementation of the MedDev Directive
- Updates from the Global Harmonisation Task Force (GHTF)
- Hear the latest updates in Electronic Vigilance pilot studies
- Learn how to perform trend and periodic reporting
- Understand better how and why PMS is needed in Clinical Investigations
