BAYOOSOFT Themis provides you with a validated solution for the technical documentation of medical devices and for documentation processes for quality and information security management systems. With our software, you can digitize and link your processes, reduce effort and minimize redundant data. This allows you to optimize your technical documentation in accordance with MDR and IVDR, while at the same time ensuring efficient and compliant management of your documents.
Our specialized modules cover all relevant requirements for medical devices and management systems – from risk assessment and technical documentation to compliance with international standards and regulations such as MDR, IVDR and quality and information security standards.
Efficient technical documentation of medical devices according to MDR and IVDR
While regulatory requirements, particularly in the area of technical documentation, are constantly increasing, the world of work is becoming increasingly volatile. Topics such as collaboration, growing teams and cross-location working are indispensable components of the corporate world today.
How can you reduce effort and costs at the same time? With BAYOOSOFT Themis, the validated and standard-compliant solution for increasing regulatory productivity.
How it works: With BAYOOSOFT Themis, your technical documentation processes are digitized and accelerated through central management and the linking of individual information units. This optimizes not only individual tasks, but also complete process chains.