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Council and Parliament representatives confirm agreement on medical device and IVD regulations


Press release Brussels, 15 June 2016 – The medical technology industry welcomes the vote on the consolidated medical device and in vitro diagnostics regulation texts by representatives of the Council and the Parliament today. The Environment, Public Health and Food Safety (ENVI) Committee of the European Parliament and Council’s Committee of Permanent Representatives (COREPER) voted

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Novosanis: vacancy MedTech Product Developer


Novosanis is a young, dynamic and innovative medical device company which was founded in March 2013. We are looking for a MedTech Product Developer to strengthen our Design & Engineering team. Novosanis has two device platforms, VAX-ID suited for injection of e.g. vaccines in the dermal layer of the skin, and Colli-Pee suited for guaranteed

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Eerste Galenusprijs ‘medical devices’ voor implanteerbare defibrilator.


De Galenusprijs bekroont innovatie in de gezondheidszorg. Binnen de farmaceutische industrie geniet de Galenusprijs een goede reputatie. Voor het eerst organiseert Artsenkrant dit jaar een Galenusprijs voor het ‘meest betekenisvolle innovatief medisch hulpmiddel van 2015′. Een terechte en positieve evolutie aangezien innovatie dé driver is in onze sector. Lees het volledig interview met dhr. Richard

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Council and European Parliament reached political agreement on the medical devices and in vitro diagnostic medical devices regulations


Brussels, 26 May 2016 – Following the May 25th trilogue meeting, MedTech Europe, the alliance of Eucomed and EDMA, are pleased to hear that a political agreement has been reached on the new regulations. The two regulations on medical devices and in vitro diagnostics include measures which will have a significant impact on patients, regulators

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Register now for the workshop “Personalized Medical Devices” (23/6/2016)


On Thursday June 23rd at 11:30pm MedTech Flanders invites its members to present and share lessons learned and good practices as well as debate on pitfalls and open issues in regulations concerning personalised medical devices. This workshop will be lead by Ward Callens, MBA – director of qualitiy at Materialise and hosted by Cochlear (Mechelen). Participation is free for

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