Program
Invention, innovation and Entrepreneurship;
Protection of intellectual property;
Roles and responsibilities: manufacturers, agents, importers and distributors, responsible person;
Essential requirements;
Conformity assessment and CE marking;
Supporting documentation of a DM (technical Dossier, EC Declaration Of Conformity, EC Certificate of Conformity);
Preclinical assessment, clinical evaluation and bibliographic evidence;
Marketing requirements for DMs (registration of DMs in the INFARMED portal…);
Monitoring and surveillance of the market.
Internship(s)
NAO