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The European Medical Device Regulation (MDR) defines strict requirements for the approval and placing on the market of medical devices. In addition to detailed chemical characterization, comprehensive proof of biocompatibility is also required.

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What a day! We are still deeply impressed by the great response to our first OMPG OpenHouse event! The large number of participants and the lively…

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Fire safety is an important quality feature - not only for buildings, but also for consumer goods, semi-finished products and raw materials. For more…

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As part of the consulting guidelines of the Free State of Thuringia, our company receives funding for consulting and process support. These support…

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We would like to show you what we can do! On Wednesday, March 19, 2025, we cordially invite you to Rudolstadt. You can look f…

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Environmental influences can have a major impact on the function and service life of coated materials, components and packagi…

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"Plasticizers and PAH findings in toys and body contact materials", "Hazardous chemicals in cosmetics", "EU states call for p…

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The "STEM-friendly school" award has been a permanent fixture here for years; participation in "Youth researches" projects is…

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After several participations in the Medica medical technology trade fair, we have now decided to take part in the Compamed su…

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As one of three test laboratories in Germany, OMPG is again approved by Volkswagen AG for the complete range of emission test…

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