Training
Understand and apply risk management for medical devices with ISO 14971:2019
RDM, in vitro, 13485, management, gestion, risk, benefit, ISO 14971, clinical, software, PMS, SAC, SCAC, technical documentation, post-market surveillance, usability, safety, security, performance, manufacturer, subcontractort
The software lifecycle (IEC 62304) in the context of CE marking for medical devices
RDM, MDR, 13485, IA, intelligence artificielle, AI, software, DHF, DMR, technical documentation, post-market, risk, ISO14971, class, classification, requirements, security, performances, medical device, manufacturer, management, ISO13485, 62304