ICCAS recertified 05.01.2022
Companies can continue to implement cooperation projects with ICCAS according to the German Medical Products Law DIN EN ISO 13485. This is ensured by the successful ISO recertification, which was renewed for ICCAS’ research and development of medical device software. For companies, this means that the software systems developed in cooperation with ICCAS fulfil the requirements of quality standards of the medical products law and can be implemented by purpose. Production processes and methods take place under defined guidelines, which ensure a high quality of the products.