TECHNOVIGILANCE

Crt dispositivos médicos

We provide consulting services from the implementation of a post-market surveillance unit for the reports required for registration renewal.
In the past few years, a new international post-market vigilance system for medical devices has been implemented for manufacturers, distributors, hospitals and users. In Mexico, technovigilance is mandatory and needed for registration renewals. Our technovigilance services include:

Implementation of a Technovigilance Unit (NOM 240 SSA1 2012 – Mexico)

Personnel Training about

Technovigilance

Technovigilance reports for medical devices health registrations’ renewal in Mexico

Post-market vigilance reports to comply with CE brand registrations