QualityDRG works according to EN ISO 13485:2016 standard, certified by TÜV Rheinland Product Safety GmbH, an indication of our commitment to customer service, quality control and improved health care. We participate in a number of quality assessment schemes, which included INSTAND e. V., Germany, RfB (Referenzinstitut für Bioanalytik), Germany, as well as DEQAS (Vitamin D External Quality Assessment Scheme), Great Britain. DRG products meet the essential requirements of the directive 98/79/EC of 27. October 1998 on in-vitro diagnostics medical devices.
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