Next Thursday, 3 November, the Spanish Federation of Healthcare Technology Companies (FENIN) organises, in conjunction with the Spanish Agency for Medicines and Healthcare Products (AEMPS), at the Foment del Treball Nacional headquarters in Barcelona, a training session on the new European regulations concerning Medical Devices and In Vitro Diagnostic Medical Devices, which is due to be approved in early 2017.
The information session is entitled “Information session on the new European regulations on medical devices”. It will begin with a presentation by Jose Luis Fernández, president of FENIN Catalonia. This will be followed by presentations from Maria Carmen Abad Moon, Head of the PS Department at AEMPS, Francisco Sevilla Pérez, Counsellor for Health and Consumer Affairs at the Permanent Representation of Spain to the European Union, and Maria Concepción Rodríguez Mateos, Head of the Medical Devices Department at the AEMPS. Finally, the closing address will be given by María Aláez Usón, Technical Director at Fenin.
A new Medical Devices Regulation
From the Gabinete Técnico Farmacéutico M. Camps, we would like to recommend that you take part in this training session on the new European regulations. If you plan to attend the event, you can download the registration form here, or write to m.gonzalez@fenin.es to find out more about the event.