Changes to the questions and answers and guidance document on mobile technologies
Swissmedic updated its Q&A and guidance document on mobile technologies.
Swissmedic · SwitzerlandSwissmedic
Regulation
Category
Type
Date
swissdamed: Mandatory registration of medical devices and in vitro diagnostic medical devices as of 1 July 2026
Mandatory registration of medical devices and in vitro diagnostic medical devices in the Swiss registry (swissdamed) enters into force.
Swissmedic · SwitzerlandNew guideline: Swiss Good Practice for Post-Market Surveillance of In-Vitro Diagnostics (GPMV-IVD)
Swissmedic publishes new guideline on post-market surveillance practices for in-vitro diagnostic devices.
Swissmedic · SwitzerlandUpdating of the information sheet Guidance for Industry on the electronic exchange of ICSRs in E2B(R3) format through B2B gateway
Updated guidance on electronic exchange of individual case safety reports in E2B(R3) format via B2B gateway.
Swissmedic · Switzerland
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