Products with the CE marking to identify consumers that the products meet the stringent requirements of the European Directives, both in its production process, as in quality control.

FDA is the government body in the United States of America that controls, tests and studies on products before having their tradable approved in their country.

The Good Manufacturing Practices (GMP) requirements used as the basis of Resolution Collegiate Directive Number 59 of 2000 (59:2000 DRC), which assigns criteria to ensure that the processes and quality inspections in an Industry conform to appropriate release of a quality product to the market, as well as their constancy reproducibility.

Health Products - Quality Management Systems.
The ISO system shows that an organization has the capacity to provide products and associated services that consistently satisfy quality requirements.

Quality Management Systems