Rethinking technical documentation
As regulatory requirements continue to rise, the world of work is becoming increasingly volatile. Topics such as collaboration, growing teams and working across locations are now commonplace in the world of medical device manufacturers. This is precisely why BAYOOSOFT Themis is reshaping the path of technical documentation – holistically, innovatively, individually and globally.
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. This significantly reduces the use of resources and error rates compared to manual processing. In this way, operational expenses, for example when updating existing files, can be sustainably reduced. At the same time, the acceptance and quality of the documentation created is improved and compliance with MDR and IVDR requirements is ensured.
The features of BAYOOSOFT Themis at a glance
The BAYOOSOFT Themis modules
Efficient technical documentation of medical devices in accordance with MDR and IVDR and optimized process management with ISMS and quality management software.
