Last updated: 30 September 2026 The Master UDI-DI groups specified highly individualised medical devices according to relevant design parameters. It reduces the number of identifiers to be registered in EUDAMED…
Must a Swiss hospital or medical practice register a CE-compliant medical device in swissdamed if it is sourced directly from the EU? Not automatically. The decisive factor is not the…
Regulatory software creates the greatest value not by offering as many functions as possible, but by supporting a specific process reliably, transparently and with clear responsibilities. A recent article by…