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. Assistive technology: definition and safe use

  2. MHRA fees

    • MHRA
    • Statutory guidance
  3. Drug Safety Update: monthly PDF newsletter

    • MHRA
    • Guidance
  4. Common issues identified during clinical trial applications

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

  6. E-learning modules: medicines

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

  8. Guidance on GxP data integrity

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

  10. Out-of-specification investigations

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

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

  13. Guidance on applying human factors to medical devices

    • MHRA
    • Guidance
  14. Widening the availability of naloxone

  15. Notified bodies for medical devices

  16. Medical devices: Virtual Manufacturing replaces Own Brand Labelling

  17. Medical devices regulations: compliance and enforcement

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

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

  20. Reporting adverse incidents: coronary stents

  21. Parallel imports of medical devices

    • MHRA
    • Guidance
  22. Single-use medical devices

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

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

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

  26. Baseline guidance for medicine licence submissions

    • MHRA
    • Guidance
  27. Electrosurgery: top tips

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

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

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

    • MHRA
    • Guidance
  31. DEHP phthalates in medical devices

  32. Lasers, intense light source systems and LEDs

  33. Reproduce or re-use MHRA information

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

    • MHRA
    • Guidance
  35. Managing medical devices

  36. Regulatory research dementia workshop conclusions

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

    • MHRA
    • Guidance
  38. How to use RamaXL

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

  40. Borderlines between medical devices and medicinal products

    • MHRA
    • Guidance