QualityDRG works to EN ISO 9001:2008 and EN ISO 13485:2003+AC:2007 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 (Germany) and Dt. Ges. für Klinische Chemie, DGKL, Germany. DRG products meet the essential requirements of the directive 98/79/EC of 27. October 1998 on in-vitro diagnostics medical devices. Certificates: EN-ISO-13485-2007 DE EN-ISO-13485-2007 EN EN-ISO-9001-2008 DE EN-ISO-9001-2008 EN ISO 13485-2003 under CMDCAS AEO Certificate |
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