Newsletter

Joint industry statement on harmonised Waste Sorting Instructions for packaging

MedTech Europe joins the European Framework for Advanced Medical Technology Evaluation and Follow-up Stakeholders Forum

Just published: amending electronic Instructions for Use regulation for medical devices

Revision of Standardisation Regulation 1025/2012

EU green lights restriction to EU public procurement for medical devices and companies from China

News from the World Health Organisation, and from the Global Diagnostics Alliance to the World Health Organisation Global Forum on Medical Devices

A look back at The MedTech Forum 2025

European Medical Device Nomenclature required for Medical Device Regulation and In Vitro Diagnostic Regulation submissions

Updated – Innovative Health Initiative draft topic texts for Call 11

MedTech Europe recommendations to the upcoming Danish Presidency of the Council of the European Union

7 years of General Data Protection Regulation : protecting privacy and strengthening patient trust

EuroMedLab conference: MedTech Europe joins Symposium on green and sustainable medical laboratories

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