Validation for Medical Devices

Quality assurance in the reprocessing of medical devices

Our high professional standard in the fields of cleaning, disinfection and sterilisation enables you to benefit from a team of qualified application engineers. When validating reprocessing processes, the focus is on quality assurance measures and therefore the existence of reproducible processes when preparing medical devices. We assist you with the analysing and optimising of your preparing process. The cutting-edge measuring technology and years of experience enable us to provide you with an overview of the effectiveness of your sterile materials reprocessing and also remedy any weaknesses. The legislator demands that the cleaning disinfection and sterilisation of medical devices is to be carried out with a suitable validated procedure; this is where the German Medical Devices Act (MPG) supplemented by the Regulations Governing the Setting up, Operation, Use and Maintenance of Medical Devices (MPBetreibV) is applicable.