The Central Authority of the Federal States for Health Protection of Medicinal Products and Medical Devices recognizes that CleanControlIng Medical GmbH & Co. KG has the competence according to Regulation (EU) 2017/745 and DIN EN ISO/IEC 17025 for biological, chemical and microbiological-hygienic testing of medical devices, sterile barrier and packaging systems and substances as integral parts with adjuvant function of medical devices according to Article 1(8) of Regulation (EU) 2017/745 as well as for physical testing of sterile barrier and packaging systems and for environmental monitoring.
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