Training Pill: How to obtain the CE Mark with Medical Devices: Introduction to the EU MDR 2017/745

In order to ensure that medical devices are safe, this training lays the foundation for regulatory planning, beginning with the classification of the device, the EU regulatory ecosystem, the conformity assessment procedure, the clinical evaluation, the development of the technical documentation, and the requirements for quality management system certification and registration. This lecture will be hold by Carmen Martín, expert in ensuring that regulatory strategies.

17/03/2022 de 11:00 a 12:30
Xartec Salut CREB UPC
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