Publications: guidance

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

Filter publications
103 publications about National Health Service × and about Public health × 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. Common issues identified during clinical trial applications

    • MHRA
    • Guidance
  2. Drug Safety Update: monthly PDF newsletter

    • MHRA
    • Guidance
  3. Guidance on GxP data integrity

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

  5. Out-of-specification investigations

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

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

  8. Medical devices: software applications (apps)

  9. Guidance on applying human factors to medical devices

    • MHRA
    • Guidance
  10. Widening the availability of naloxone

  11. Notified bodies for medical devices

  12. MHRA fees

    • MHRA
    • Statutory guidance
  13. Medical devices: Virtual Manufacturing replaces Own Brand Labelling

  14. Medical devices regulations: compliance and enforcement

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

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

  17. Assistive technology: definition and safe use

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

  19. Reporting adverse incidents: coronary stents

  20. Parallel imports of medical devices

    • MHRA
    • Guidance
  21. Single-use medical devices

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

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

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

  25. Baseline guidance for medicine licence submissions

    • MHRA
    • Guidance
  26. Electrosurgery: top tips

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

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

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

    • MHRA
    • Guidance
  30. DEHP phthalates in medical devices

  31. Lasers, intense light source systems and LEDs

  32. Reproduce or re-use MHRA information

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

    • MHRA
    • Guidance
  34. Managing medical devices

  35. Regulatory research dementia workshop conclusions

    • 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