Eucomed-MedTech

Applicable à partir de janvier 2018, le Code d’Éthique Professionnelle MedTech Europe régit tous les aspects des relations de l’industrie avec les professionnels de la santé (HCP) et les organisations de soins de santé (HCO), notamment dans le cadre des congrès et événements organisés par la profession. Cette nouvelle charte de bonnes pratiques aura un impact très fort sur les congrès médicaux notamment dans le domaine du dispositif médical, découvrez dans cette Foire aux Questions, les principaux points à retenir du code MedTech Europe pour les Congrès. Pour consulter cette FAQ

A physician-industry transparency system that requires the medtech sector to disclose publically the payments and transfers of value it makes to physicians and certain other providers is very welcome, but not in its current form. That was the conclusion drawn from yesterday morning’s opening panel discussion on global transparency which, among other things, examined different transparency models around the world, company concerns, and best practices when addressing emerging requirements. The United States, France, Belgium, the Netherlands, and other countries have enacted or are currently contemplating the implementation of such systems. While the session’s panelists agreed that a transparent future was …

By Thomas Sullivan – Policy & Medicine Members of both the European Diagnostic Manufacturers Association (EDMA) and the European Medical Technology Industry (Eucomed) approved a new Code of Ethical Business Practice. Both associations are members of MedTech Europe who are working to set high ethical standards for the medical technology industry all throughout Europe. This new Code will replace the EDMA and Eucomed codes of business practice and will be known as the MedTech Europe Code of Business Practice. This decision to adopt a common and wide-reaching code was prompted by the fact that EDMA and Eucomed each had different …

Brussels, 2 December 2015 Members of the European Diagnostics Manufacturers Association (EDMA) and of the European Medical Technology Industry (Eucomed), both members of MedTech Europe, have approved a new Code of Ethical Business Practice at their General Assemblies held on 2 December in Brussels, in a continuous effort to set high ethical standards for the medical technology industry across Europe. EDMA and Eucomed members have adopted a new common Code of Ethical Business Practice, in a move to put forward clearer and more stringent self-regulation. The code will replace the EDMA and Eucomed codes of business practice and will be …

Ce mois de juin a été marqué par une avancée concernant les deux projets de règlements visant à moderniser les règles de l’UE relatives aux dispositifs médicaux (DM) et aux dispositifs médicaux de diagnostic in vitro (DIV), déjà évoqués sur notre site. Le 19 juin, le Conseil a arrêté sa position de négociation sur le fond. Cela lui permettra de donner à la présidence luxembourgeoise un mandat pour entamer les discussions avec le Parlement européen. Pour lire l’article paru dans JIM.fr