The company's core activity is to provide services for the approval and compliance of medical devices and in-vitro diagnostics (IVDs) on international markets. This includes in particular: consulting and support for compliance with standards and regulations, conducting gap analyses and traceability analyses, developing and optimizing quality management systems (QMS), creating and optimizing technical documentation, cybersecurity consulting for the MedTech industry, and supporting the digital transformation of QMS and the development of QMS for digital health and AI products.