Rethinking technical documentation
Technical documentation rethought – efficient and compliant with standards
EffizientNormkonform
Your validated solution for documentation processes of medical devices and in vitro diagnostics – Digitize linked processes and sustainably reduce documentation efforts while minimizing redundant data.
Your validated solution for documentation processes of medical devices and in vitro diagnostics – Digitize linked processes and sustainably reduce documentation efforts while minimizing redundant data.
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 minimize both effort and costs? With BAYOOSOFT Themis, the validated and standards-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 standards-compliant technical documentation—BAYOOSOFT Themis makes this possible with the following features:
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