We develop and manufacture our products working with the highest standard of quality, by applying severe international standards, such as ISO 13.485 and Directive 93/42 (CE), besides Good Manufacturing Practices (GMP). This is quality that enables our products to be used in over 30 countries, in the most renowned medical centers.
Another Micromar conquest, the CE mark, represents the declaration that our products accomplish the exigences of European Legislation expressed in the specific policies for medical products and, thus, has free commercialization in European Union countries.
Our company certification in Good Manufactoring Practices (GMP) of medical products is driven to guarantee our product's highest levels of quality, safety and efficacy, commercialized in worldwide ambit. It's implementation ensures that Micromar practise an applied vigilance over project, manufacture, packing, storage, inspection and trials procedures, as well as inatallations and technical assistance of the medical products.
The objective is to promote the processes and services standardization, for the continuous quality improvement.This norms stablish requirements which assist the progress of the internal processes, the monitoration in work environment, the best capacitation of our collaborators, the satisfaction verification of customers, collaborators and furnishers,in a continuous process of quality management improvement.
Food and Drug Administration certification, one of the strictest certifications in the world, was given to Micromar in 2015, with the EasyDrill Cranial Perforator project. As part of its strategy, Micromar intends to expand certification to the other products in its line.