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NBR ISO 9001:2000 Quality Management Systems |
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NBR ISO 13485:2004 Health Products – Quality Management Systems The ISO System is evidence that an organization has the capacity of providing products and the associated services that consistently fulfill quality requirements.
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CE Products with the CE mark inform the consumer that those products abide by the rigorous European guidelines, both in terms of production process as well as quality control |
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FDA – Foods and Drugs Administration The FDA is the governmental agency of the United States of America that controls, tests and studies products before approving their commercialization in the country. |
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GMP - Good Manufacturing Practices Good Manufacturing Practices (GMP) employ the requirements set by Collegiate Directive Resolution number 59 of the year 2000 (RDC 59:2000), which establishes criteria to guarantee that the quality processes and inspection procedures in an industry are adequately in conformity, prior to the launching of a quality product in the market, as well as to guarantee that such quality can be constantly reproduced. |
