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Registration of reusable or upclassified Class I devices and/or expiring CE certificates

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1. Registration of in vitro diagnostic devices with expiring CE certificates
2. Exceptional Use Authorisation
3. MHRA announces proposals to improve access to world’s best medical devices for patients and to boost economic growth in Britain’s med tech sector
4. Designated standards prioritisation
5. Government to align with European specifications on high risk in vitro diagnostic devices to reduce regulatory burden