BAYOOSOFT Themis Features

Comprehensive, innovative and global – these keywords aptly describe BAYOOSOFT Themis. But our software solution is also individual. Because that’s exactly what your requirements are. That’s why we offer you various modules and functions to help you achieve your goals even faster when creating technical documentation.

Comprehensive, innovative and global – these keywords aptly describe BAYOOSOFT Themis. But our software solution is also individual. Because that’s exactly what your requirements are. That’s why we offer you various modules and functions to help you achieve your goals even faster when creating technical documentation.

Teamwork
  • Multi-user capability
  • Collaboration through chat & comment function
  • Structured navigation through the requirements
  • browser-based
  • Team dashboards & push notifications
  • Simplified organization
Digitization
  • Fine-grained, dynamic linking of all relevant information
  • Knowledge database for cross-product synergy effects
  • Simplified document management
  • Direct start by importing unstructured data
  • digital approval workflow
Monitoring
  • Project phase-based working method with versioning
  • Audit trail to track all changes
  • Fine-grained authorization management
  • Backward search function
  • Change histories for each element
  • Data-driven dashboards for work analysis

Features

Compliant with standards: medical devices & in-vitro
Document management as a single source of truth
Editorial work on documents
Versioning & approval workflow
Audit trail & version history
Validated software environment (ISO 13485)
Generation of Technical Documentation File
Cross-site team collaboration

Modules

Documentation Guide

Who, how, what? The Documentation Guide enables you to work transparently with your documents.

Risk Manager

Risk management in accordance with ISO 14971: Whether PHA or FMEA – you are guided through all work steps in a structured manner.

Device Validation Manager

Your fast track to the release of your medical or IVD product: plan and document all tests centrally.

Requirements Engineer

Manage all requirements (MDR, IVDR, general product requirements, …) in a clear and structured way in one central location.

Svenja Winkler
CEO

How to contact us

How would you like to work in the future?

Be part of it and shape the Tech Doc of tomorrow with us. Send us a short message and our team will take care of your request immediately.