Preparation of supporting documentation of the Quality Management System in compliance with the health regulation in Mexico, its implementation and training of the documents that comprise it, according to the activities of the health-related business.
Review of products´ and/or health supplies´ labeling, as well as evaluation and analysis issuance according to the applicable Mexican Mandatory Norms that must be met.
Preparation of supporting documentation and implementation of the Techno-surveillance Unit, whose purpose is to guarantee that the medical devices available in the market, are performing according to the manufacturer´s intended use.
Compliance verification of the regulations applicable to establishments dedicated to the commercialization of health supplies.
