EU call for experts: Medical Device Regulation

Sehr geehrte DeGIR-Mitglieder,
die Medical Device Regulation, die derzeit in nationales Recht umgesetzt wird, wird gravierende Einschränkungen beim Inverkehrbringen von neuen, innovativen Medizinprodukten mit sich bringen. Die EU-Kommission sucht derzeit nach Experten für Beratungsgremien, die die Einführung der Medical Device Regulation begleiten. Der DeGIR-Vorstand unterstützt den Aufruf der CIRSE an die Mitgliedsorganisationen, sich an dem Bewerbungsprozess zu beteiligen. Informationen zur Bewerbung finden Sie in der unten im Aufruf der CIRSE und im Dokument der EU-Kommission.
Mit freundlichen Grüßen

Aufruf der CIRSE:
The European Commission has issued a call for experts to join panels providing consistent scientific, technical and clinical advice concerning the implementation of EU regulation 2017/745 on medical devices.
The eligibility criteria for applicants are:
•    Citizenship of EU/EFTA member state or Turkey
•    Medical or scientific university degree
•    10 years of relevant professional experience
•    Fluency in English
•    No financial or other interest in the medical device industry
Required commitments include:
•    Availability to carry out remote work, including teleconferences for typically 2-3 days/month
•    Availability to physically attend a meeting at least once a year
More information with regard to specific requirements, application form and the full call can be found here. Please find attached a flyer [Download-Link:] containing the most important information.
Anyone who wishes to be considered for appointment as advisor to expert panels in the first cycle of appointments must submit a completed application by 10 November 2019.
The Executive Board encourages the sharing of this information and the application of suitable candidates. Anyone who is planning to apply is kindly asked to inform CIRSE Central Office by emailing