Publications: guidance

You can use the filters to show only results that match your interests

Filter publications
103 publications by Medicines and Healthcare products Regulatory Agency ×
Get updates to this list email feed

Copy and paste this URL in to your feed reader

  1. Drug Safety Update: monthly PDF newsletter

    • MHRA
    • Guidance
  2. Supply unlicensed medicinal products (specials)

  3. Assistive technology: definition and safe use

  4. Implementation period: what it means for the life sciences sector

    • DHSC, VMD and MHRA
    • Guidance
  5. MHRA fees

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

    • MHRA
    • Guidance
  7. Medical devices: software applications (apps)

  8. E-learning modules: medicines

    • MHRA
    • Guidance
  9. Medicines: notes for applicants and holders of a wholesale dealer licence or broker registration

  10. Guidance on GxP data integrity

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

  12. Out-of-specification investigations

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

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

  15. Guidance on applying human factors to medical devices

    • MHRA
    • Guidance
  16. Widening the availability of naloxone

  17. Notified bodies for medical devices

  18. Medical devices: Virtual Manufacturing replaces Own Brand Labelling

  19. Medical devices regulations: compliance and enforcement

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

    • MHRA
    • Guidance
  21. Infections associated with heater cooler units used in cardiopulmonary bypass and ECMO

  22. Reporting adverse incidents: coronary stents

  23. Parallel imports of medical devices

    • MHRA
    • Guidance
  24. Single-use medical devices

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

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

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

  28. Baseline guidance for medicine licence submissions

    • MHRA
    • Guidance
  29. Electrosurgery: top tips

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

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

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

    • MHRA
    • Guidance
  33. DEHP phthalates in medical devices

  34. Lasers, intense light source systems and LEDs

  35. Reproduce or re-use MHRA information

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

    • MHRA
    • Guidance
  37. Managing medical devices

  38. Regulatory research dementia workshop conclusions

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

    • MHRA
    • Guidance
  40. How to use RamaXL

    • MHRA
    • Guidance