Transition Periods

Recommendations on the use of Guidance Documents

The IVD Regulation is amended to extend its transitional provisions

MedTech Europe information leaflet on UDI and implant card availability

The first module of EUDAMED on Actor registration to be launched in December

New MedTech Europe Reflection Paper, Is the IVD Regulation Framework ready for Class D Devices?

Is the IVD Regulation Framework ready for Class D Devices?

Industry reinstates its call for solutions to ensure a workable transition to the new regulatory frameworks for medical devices and in vitro diagnostics

Urgent solutions needed to ensure a successful transition to the new IVD Regulation in light of COVID-19

Ensuring a successful transition to the new IVD Regulation in light of COVID-19

MedTech Europe urges EU authorities to make IVD Regulation implementation workable

Implementation tools to help transitioning from Directives to Regulations

Industry Perspective on the Implementation Status of the MDR/IVDR

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