Implementing the new IVD and Medical Devices Regulations – Resourcing and Governance –

MedTech Europe urges the European Commission and Member States to invest additional resources needed to successfully implement the new In Vitro Diagnostic (IVD) Medical Devices and Medical Devices (MD) Regulations. The association also urges to clarify the new governance system under which guidance and secondary legislation will be developed and to ensure the early and meaningful involvement of stakeholders.