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Meta descripción Conoce qué es la EMDN (European Medical Device Nomenclature), su función dentro del Reglamento Europeo de Productos Sanitarios y...
RECOPS is the new application for the marketing authorisation of medical devices, created by the AEMPS.
The regulatory environment for medical devices in Spain faces an immediate and far-reaching operational change. The Spanish Agency for...
Medical devices are devices that have a medical-health purpose, but no principal pharmacological action. They are part of our daily life
The PubSanDi Programme was created with the publication in the Diari Oficial de la Generalitat de Catalunya of Resolution SLT/1258/2024, which created the Programme for monitoring the advertising of medical devices, cosmetics and products with purported health purposes in the digital environment.
The Council of Ministers yesterday approved the text of the new Royal Decree on Medical Devices for in vitro diagnostics. This new RD 55/2025...
Nit de CataloniaBio & HealthTech is a networking dinner organised in Barcelona by the biomedicine and health cluster, CataloniaBio & HealthTech.
Royal Decree on Medical Devices - On 20 March, the Spanish Government, through the Council of Ministers, approved the new national regulation on Medical Devices: Royal Decree 192/2023, of 21 March, which regulates medical devices. This regulation will allow the Spanish government to update its legislation to the European Commission's Medical Devices Regulation 2017/745, and to legislate on those points where the Regulation leaves room for national authorities.
The Register of Persons Responsible for Placing Medical Devices on the Market allows manufacturers of Class I and custom-made medical devices to notify the medical devices they place on the market. Do you want to know how the register works and what information you can find in its database? Read on!
Health technologies have allowed the last two decades to see a rapid development of health services, their internal organisation and the equipment used for the diagnosis and treatment of patients.
The MedTech Forum 2022: the European employers' organisation MedTech Europe organised an international congress on health technologies in Barcelona. Almost 1,000 professionals - including experts, companies, stakeholders and authorities related to the field of health technologies - took part in the annual edition of The MedTech Forum from 3 to 5 May.
Eudamed is a database created by the European Commission to control and register all medical devices marketed in the Eurozone.