Publications: guidance

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104 publications about National Health Service × and about Public health × by Medicines and Healthcare products Regulatory Agency ×
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  1. Drug Safety Update: monthly PDF newsletter

    • MHRA
    • Guidance
  2. Patient group directions (PGDs)

    • MHRA
    • Guidance
  3. Devices which incorporate an ancillary medicinal substance

  4. Medical devices: software applications (apps)

  5. Guidance on applying human factors to medical devices

    • MHRA
    • Guidance
  6. Toolkit on the risks of valproate medicines in female patients

  7. Widening the availability of naloxone

  8. Notified bodies for medical devices

  9. MHRA fees

    • MHRA
    • Statutory guidance
  10. Common issues identified during clinical trial applications

    • MHRA
    • Guidance
  11. Medical devices: Virtual Manufacturing replaces Own Brand Labelling

  12. Medical devices regulations: compliance and enforcement

  13. Leadless cardiac pacemaker therapy:new guidance from an MHRA Expert Advisory Group

    • MHRA
    • Guidance
  14. Herbal medicines granted a traditional herbal registration (THR)

  15. Infections associated with heater cooler units used in cardiopulmonary bypass and ECMO

  16. Assistive technology: definition and safe use

  17. Medicines: notes for applicants and holders of a wholesale dealer licence or broker registration

  18. Reporting adverse incidents: coronary stents

  19. Parallel imports of medical devices

    • MHRA
    • Guidance
  20. Single-use medical devices

    • MHRA
    • Guidance
  21. Magnetic resonance imaging equipment in clinical use: safety guidelines

  22. Occupied wheelchairs in cars and private transport – reminders of safe use

    • MHRA
    • Guidance
  23. Adverse incidents: cardiac ablation catheters

  24. Baseline guidance for medicine licence submissions

    • MHRA
    • Guidance
  25. Electrosurgery: top tips

    • MHRA
    • Guidance
  26. What is a biosimilar medicine?

    • MHRA
    • Guidance
  27. Clinical trials: how NHS trusts and health boards can maintain compliant electronic health record systems

    • MHRA
    • Guidance
  28. Good laboratory practice (GLP) facilities: risk-based quality assurance

    • MHRA
    • Guidance
  29. DEHP phthalates in medical devices

  30. Lasers, intense light source systems and LEDs

  31. Reproduce or re-use MHRA information

    • MHRA
    • Guidance
  32. Field safety notice (FSN): what it is and why it's important

    • MHRA
    • Guidance
  33. Managing medical devices

  34. Regulatory research dementia workshop conclusions

    • MHRA
    • Guidance
  35. Good manufacturing practice: data integrity definitions and guidance

    • MHRA
    • Guidance
  36. Guidance for 'specials' manufacturers

    • MHRA
    • Guidance
  37. How to use RamaXL

    • MHRA
    • Guidance
  38. Adverse incidents: in vitro diagnostic (IVD) blood glucose meters

  39. Borderlines between medical devices and medicinal products

    • MHRA
    • Guidance
  40. Borderlines with medical devices

    • MHRA
    • Guidance