Nexo MedTech is a regulatory consulting firm specialising in EU MDR (Regulation 2017/745), supporting medical device manufacturers in achieving and maintaining CE marking across Europe.
We combine regulatory expertise with modern tools to accelerate document production, clinical evaluations, technical documentation, PMS/PMCF plans, without compromising scientific or regulatory rigour.
We work with SME manufacturers across Spain, Italy, D-A-CH, the UK, and international markets, with a focus on Annex XVI devices, Legacy MDD-to-MDR transition, and Software as a Medical Device (SaMD).

Nexo MedTech

Org chart

Teams

Offices

Nexo MedTech

Org chart

Teams

Offices

Related companies