Since the very beginning TOMTEC has established itself as a solution provider for the medical industry. Sharing our experience in analysis, quantification and management of medical images is part of our company mission.
Therefore we know what it means to be a qualified and reliable cooperation partner.
Our Quality Management system has been approved and certified to comply with the requirements of EN ISO 13485:2016 as well as MDSAP. TOMTEC as a recognized medical industry partner considers it essential to comply with international quality system regulations, such as required in EU Regulation 2017/745 (MDR) and US Quality System Regulation 21 CFR 820.
Our certified & regulatory cleared product offerings give you access to the global market place.
Referring to existing TOMTEC product clearances makes it easier for you when you register TOMTEC modules as integrated part of your product. Multi-language support for any level of integration is a self-evidence for us.
Our Modular Solution Concept makes it easy to pick and choose the adequate way of integration – whether as full application or just a single module. Different types of predefined interfaces facilitate quick adaptation & customization, ensuring a short time-to-market.