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Medical devices: get regulatory advice from the MHRA

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  1. Medicines and Medical Devices Act 2021 – Stakeholder survey
  2. MHRA guidance on new Medical Devices Post-Market Surveillance requirements
  3. MHRA outlines intent to speed up patient access to innovative medical devices
  4. Designated standards prioritisation
  5. Consultation on the Revised International Council for Harmonisation Guideline M4Q(R2)