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  1. Send and receive information on adverse drug reactions (ADRs)

    • Updated
    • Detailed guide
    • MHRA
  2. Apply for the early access to medicines scheme (EAMS)

    • Updated
    • Detailed guide
    • MHRA
  3. Good clinical practice for clinical trials

  4. Clinical trials for medicines: apply for authorisation in the UK

  5. Regulatory guidance for medical devices

    • Updated
    • Collection
    • MHRA
  6. Good manufacturing practice inspection deficiencies

    • Updated
    • Official Statistics
    • MHRA
  7. Marketing authorisations: lists of granted licences

    • Updated
    • Collection
    • MHRA
  8. Parallel import licences: lists of approved products

    • Updated
    • Collection
    • MHRA
  9. Parallel import licences granted in December 2016

  10. Marketing authorisations granted in December 2016

  11. E-cigarettes: regulations for consumer products

    • Updated
    • Detailed guide
    • MHRA
  12. Human and veterinary medicines: register of licensed wholesale distribution sites

  13. Medicines: licensing time-based performance measures

    • Updated
    • Official Statistics
    • MHRA
  14. Standards for biological medicines - understanding them and how they make a difference

    • Published
    • News story
    • MHRA
  15. Suspended and revoked licences for manufacturers and wholesalers of medicines

  16. Strategy for pharmacopoeial public quality standards for biological medicines

    • Published
    • Open consultation
    • MHRA
  17. Conferences and events

    • Updated
    • Collection
    • MHRA
  18. Human and veterinary medicines: register of licensed manufacturing sites 2016

  19. Medicines: terminated and cancelled manufacturing and wholesale dealer licences

  20. Medicines: new manufacturing and wholesale dealer licences

  21. Register of brokers authorised to deal in human medicines

  22. Early access to medicines scheme applications: pending, refused, granted

    • Updated
    • Official Statistics
    • MHRA
  23. Clinical trials for medicines: authorisation assessment performance

    • Updated
    • Transparency data
    • MHRA
  24. #FakeMeds in 2017: New Year, Same Danger

    • Published
    • News story
    • MHRA
  25. Clinical trials for medicines: manage your authorisation, report safety issues

  26. The Yellow Card Scheme: guidance for healthcare professionals

    • Updated
    • Detailed guide
    • MHRA
  27. Agency highlights 2016

    • Published
    • News story
    • MHRA
  28. MHRA statement on products containing Cannabidiol (CBD)

    • Updated
    • News story
    • MHRA
  29. Advertising investigations by MHRA

    • Updated
    • Collection
    • MHRA
  30. Advertising investigations: November 2016

  31. Medicines and Healthcare products Regulatory Agency’s staff survey results 2016

    • Published
    • Corporate report
    • MHRA
  32. Marketing authorisations granted in November 2016

  33. Parallel import licences granted in November 2016

  34. Regulator investigating the diversion of prescription only medicines

    • Published
    • Press release
    • MHRA
  35. Medicines: apply for a parallel import licence

    • Updated
    • Detailed guide
    • MHRA
  36. Count down to Christmas with the FakeMeds advent calendar

    • Published
    • News story
    • MHRA
  37. Drug Safety Update: monthly PDF newsletter

    • Updated
    • Guidance
    • MHRA
  38. Good laboratory practice (GLP) for safety tests on chemicals

    • Updated
    • Detailed guide
    • MHRA
  39. Partnership to protect public health – MHRA and HTA sign agreement

    • Published
    • Press release
    • MHRA
  40. Register a homeopathic medicine or remedy

    • Updated
    • Detailed guide
    • MHRA