DRG develops and manufactures diagnostic ELISA test kits for use in clinical and research laboratories. The experience of the production and management team guarantees to provide high quality products, competitive prices and excellent customer service.

DRG works in compliance to DIN EN ISO 13485 standard, certified by TÜV Rheinland Product Safety GmbH, an indication of their commitment to customer service, quality control and improved health care. DRG participates in a number of quality assessment schemes, which include Instand (Germany) and RfB (Germany). DRG products meet the essential requirements of the directive 98/79/EC of 27th October 1998 on in-vitro diagnostic medical devices.