Use the organisation document library
Find uploaded manufacturer sources without confusing them with case outputs.
Technical file and documents
Where to find it
DocumentsYou need
- A client organisation with uploaded or declared documents.
The library lists manufacturer source documents and their control information. A generated case document belongs to its case workflow and is not made authoritative by sharing a similar title.
Clicking a row previews the file. The declaration and controls are behind the row's ⋯ menu — "Download", "Edit metadata" and "Delete". Use the case page for the generated technical-file output.
What happens next
- Attach or select the controlled source from the case workflow that needs it.
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Official references
This article is practical product guidance, not legal advice. Confirm regulatory deadlines and obligations against current official sources and your assigned expert.
European Commission — Medical Devices: New regulationsRegulation (EU) 2017/745 — Medical Device RegulationRegulation (EU) 2017/746 — In Vitro Diagnostic Medical Devices