Actualización en investigación con productos sanitarios tras la implantación de la regulación europea (MDR)

Despite the 2017 update to European medical device regulation and its entry into force in 2021, many doubts persist about its real-world application in medical device (MD) research in Spain. The development of MDs requires collaboration among numerous stakeholders, including researchers, ethics committees, notified bodies, the Spanish Agency of Medicines and Medical Devices, manufacturers, and other involved parties-all of whom have had to adapt to the new regulatory framework. This has required a significant effort and consumption of resources to understand and apply the different clinical practice guidelines to unify protocols in MD research and ensure the safety and efficacy profile of these products. Although challenges remain, the adoption of this legislation has fostered collaboration among stakeholders, enabling progress and a better understanding of the new obstacles it presents. The aim of this review is to define, in a practical way, the content of this regulation and expose the perspectives of the different actors involved in the development of MD.