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

During the challenging times of the COVID-19 pandemic, medical device manufacturers are striving to keep clinical investigations for existing and new medical technologies running with minimal disruption while preserving the safety of the participants and the quality of the generated data. Despite the best efforts, some activities in the framework of clinical investigations may have to be delayed, slowed down or reduced. In view of this situation and its potential impact on recertification of medical devices joint efforts are needed from all stakeholders. To find out more we invite you to consult the MedTech Europe statement on the matter.