Marc Benet Pozo

I’m co-founder of a medical device startup, and also, As a QA/RA Manager, I am in charge of obtaining the CE marking for our medical devices under MDR 2017/745, developing and implementing the Quality Management System in the company, ensuring compliance with National and European regulatory requirements in product approval/commercialization/labelling, and planning and maintaining the quality standards that apply to the company’s products, always following the standards of the medical device industry (ISO 13485, ISO 14971, IEC 60601, etc.)