Important topics of the Medical Technology Committee are:
- European Regulation for Medical Devices EU 2017/745 (MDR)
- European Regulation on in vitro diagnostic medical devices (EU) 2017/746 (IVDR)
- Other New Legislative Framework (NLF) legislation such as Machinery Regulation, Low Voltage Directive, Radio Equipment Directive (RED), Blue Guide and others
- Unique Device Identification (UDI)
- Eudamed
- Standards
- International matters, IMDRF
- Cybersecurity and Artificial Intelligence
- Digital Health
- Electronic instructions for use
- Environmental and circular economy legislation (e.g. Green Deal, Circular Economy Action Plan, Chemical Strategy for Sustainability, in particular but not limited to WEEE, ROHS, REACH, CLP, Biocidal Products Regulation, POP Regulation, Eco-design, Battery Regulation, Green claims, Packaging, SCIP)
- Market development/ statistics in Europe and worldwide