Survey sector
on the basis of members data are available in documents 2015
NB-Med meeting
NB-Med meeting On 14th and 15th April will take place the meeting with representatives of Notified Bodies. The meeting is held in two parts. The first part is a meeting with representatives of Notified Bodies only and the second part of the meeting will take place with representatives of Notified Bodies, of the Industry association [...]
Meeting at the US embassy
April 7th Meeting at the US embassy at the initiative of Senator Alexander to present an overview of how EU notified bodies work, including some of the challenges which are being addressed through new measures, guidance and better communication among the various stakeholders/regulators.
Conference
Françoise Schlemmer is giving a conference at Euromcontact Regulatory Affairs meeting (Brussels) : Presentation of the changes and impact of the upcoming Medical Device regulations
Team-NB representatives
attend European Coordination Meeting on the International Medical Devices Regulators Forum (IMDRF) Activities.
Team-NB representatives
participate at the Vigilance Medical Devices Experts Group CWorkshop.
The Code of Conduct version 4.0
is in progress. A working group is going to meet on February 4th in Cologne. They will take into consideration the non conformities from joint audits.
Proposal
Proposal for a Regulation of the European Parliament and of the Council on medical devices and in vitro diagnostic medical devices. The Presidency's progress report will be sent to the Council (EPSCO) for its meeting on 1 December. The Council will be invited to instruct the Council preparatory bodies to continue the work with the [...]
MDEG
The MDEG meeting took place in Brussels under the chairmanship of Erik Hansson and Gert Bos, Hans-Heiner Junker and Françoise Schlemmer as representatives of the notified bodies.