That‘s what it’s all about:
The BAYOOSOFT Themis Documentation Guide supports you in creating your technical documentation according to Medical Device Regulation 2017/745 (MDR) and prevents redundancies by centralizing your documents. Each document is represented as a task, these are linked to each other, thus ensuring a single source of truth.
The web-based and structured solution guides you through technical documentation in accordance with MDR – from start to submission. After completion, you receive the initial document for the notified body, which bundles all individual documents.