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In July 2008 DQS Medizinprodukte GmbH was founded as a 100% subsidiary of DQS Holding GmbH, having already been established in 1995 as DQS Competence Center for Medical Devices and approved as Notified Body (identification number 0297) by the ZLG (Central Authority of the German Länder for Health Protection with regard to Medicinal Products and Medical Devices). DQS MED, for short, is also accredited by the German Accreditation Body (DAkkS) and the Standards Council of Canada/ Health Canada (SCC) for the ISO 13485 standard. We also offer Medical Device Single Audit Program (MDSAP) and Technical Cooperation Program (TCP lll) procedures.

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Author
Karlheinz Kohl

In his function as Head of Marketing/Sales Karlheinz Kohl with his team is responsible for the market development and the acquisition of new customers for DQS Medizinprodukte GmbH. As Regulatory Affairs Manager he is in charge of a part of our ISO customers in the non-regulated area. As lead auditor, he conducts audits on the ISO 9001, ISO 13485 and EFQM models in the metal, mechanical engineering, electrical/plastics engineering and data processing industries, among others.

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