COVID19 acute

MedTech Europe’s recommendations on testing as Europe enters the winter season

Is the IVD Regulation Framework ready for Class D Devices?

Coronavirus emergency vs. GDPR security standards (COVID-19 Q&A)

MedTech Europe Code Guidance on COVID-19 Emergency Support (27 March 2020)

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

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 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

Access to medical technologies and services during the COVID-19 pandemic – Diabetes

The Medical Technology Community Stands with Patients – Access to Medical Technologies and Services During the COVID-19 Pandemic

European Industry trade and supply chain needs to respond to Covid-19

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