COVID19

Reflection paper on Sustainable and Effective Stockpiling for Emergency Preparedness

Medtech industry supports health systems preparation in managing the increase in COVID-19 cases in Europe

IVD Industry Calls for Clear Testing Protocols to Prepare for the Winter Season during the COVID-19 pandemic

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

Medtech industry continues to work to manage the impact of the COVID-19 pandemic

MedTech Europe Position Paper addressed to EU Authorities advocating for ‘virtual’ IVDR/MDR audits

The need for ‘virtual audits’ under the Medical Device and In Vitro Diagnostic Regulations in the context of a pandemic, such as COVID-19

COVID-19 recovery: Guidance for the Re-entry of Medical Technology Representatives in Healthcare Facilities

Medtech industry is committed to support deconfinement efforts

COVID-19 Implications for Clinical Investigations Needed for Medical Device Recertification

Responding to the COVID-19 Pandemic: the Diagnostic Industry Angle

Protective Equipment in the context of COVID-19

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