Yesterday took place in Madrid the event “Medical device: from design to market release, what do I need to know?”
It was an interesting day, organized by Intertek Spain and headed by Belén de Rábago, which addressed key issues for all professionals in the sector.
Experts from different organizations and companies shared their vision and experience on the complete process of commercialization of medical devices: from initial planning to technical evaluation and market launch.
Our Technical Director of the Clinical Evaluations Department, Montse Ortega Doménech, took part in this event with a presentation in which she spoke about clinical research in the new MDR, the changes that have occurred, the challenges and challenges of a CRO in the approach to studies in this new MDR, and about the day-to-day work of a CRO and its advice to companies.
