As regulatory requirements continue to rise, the world of work is becoming increasingly volatile. Issues such as collaboration, growing teams and cross-site working are now commonplace in the world of medical device and in vitro diagnostics manufacturers.

How can you keep efforts and costs as low as possible at the same time? With BAYOOSOFT Themis, the validated and standard-compliant solution for increasing regulatory productivity.

Here’s how it works: Processes are digitized and accelerated through the central management and linking of individual information units. Not only individual tasks, but entire process chains are thus optimized. As a result, the use of resources and error rates are far lower than with manual processing. As a result, you could sustainably reduce operational efforts, e.g. when updating existing files. At the same time, you increase the acceptance of the developed files by your notified body.

Efficient and standard-compliant technical documentation – BAYOOSOFT Themis enables you to do this with the following features: