We lead companies analyzing and improving their process landscape. We show you how do develop and implement best strategies to meet regulatory requirements and to beat the market.
Starting with the PMS data collection and analysis up to the data evaluation, our service includes the full range of post market surveillance activities and monitoring for medical device manufacturer.
We support companies in the development and CE mark registration of of medical devices throughout all design phases to meet MDR and IVDR compliance and to shoorten time of CE mark approval.
We provide professional inhouse training tailored to your needs.
