Timings of the ongoing debating schedules and milestones for the statutory instrument (SI) regulating the pre-market phase of medical devices used in Great Britain have been revised. A new roadmap updates the January 2024 series of target dates.
Great Britain Pre-Market Device Regulations Reset For Late 2025
Agency To Weigh Stakeholder Views On Accepting EU Certificates
UK MHRA updates timings for key elements of the new system of medtech regulation in Great Britain and prepares to assess IVD sector views.
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