Medical Device Regulatory EU MDR, CE, FDA, MHRA, UKCA, ISO 13485 specialist
Stati Uniti
Inglese, Tedesco, Italiano, Francese
Alcune informazioni sono riportate in lingua inglese.
Chi sono
I help medical device companies navigate regulatory requirements and prepare practical, audit-ready compliance documentation for global market access. My focus includes EU MDR, CE marking, UKCA, MHRA, FDA, ISO 13485, ISO 14971, EUDAMED, technical documentation, risk management, labeling, PMS and regulatory submissions. I work with startups, manufacturers and international businesses to identify compliance gaps, organize documentation and build clear regulatory pathways.... Continua a leggere