MDR 2017/745 Guidance on commision guidance documents
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Guidance: Conformity assessment rpocedures for protective equipment July 2020

Guidance: How to verify that medical devices and personal protective equipment can be lawfully placed on the EU market and thus purchased and used - also in the COVID-19 context May 2020

Guidance on regulatory requirments for medical face masks June 2020

Guidance on medical device, active implantable medical devices and in vitro diagnostic medical devices in the COVID-19 context April 2020

Conformity assessment procedures for 3D printing and 3D printed products to be used in a medical context for COVID-19