Why BAYOOSOFT Themis?
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.
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 we rely primarily on:
| Teamwork | Digitalization | Monitoring |
|---|---|---|
| collaboration through commenting function | fine-granular, dynamic linking of all relevant information | project phase based approach with versioning |
| structured navigation through the requirements | knowledge base for cross-product synergy effects | audit trail covering all changes |
| browser based | simplified document management | fine-grained access management |
| simplified organisation | change history on every element |
What areas of application are covered?
Compliance with regulatory requirements is necessary in a wide variety of situations. This is why we support you with BAYOOSOFT Themis in answering the following questions:
- Which documents (still) need to be processed?
- What is the current status of the documentation process?
- And who is responsible for which task?
We enable you to finde these answers for the following application scenarios:
- Generating the Technical Documentation for Medical Devices (incl. In-Vitro Diagnostics))
- Create and maintain Management Systems
Would you like to receive assistance for other application scenarios? Then have a look at our roadmap - we may be working on it already. Or give us feedback on which scenario is the most exiting for you.
First Steps - What's next?
Take a look at our Themis 1x1.
Do you have any further questions? Here you will find the contact to our Service Team.