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  1. Suspended and revoked licences for manufacturers and wholesalers of medicines

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

    • Updated
    • Detailed guide
    • MHRA
  3. Help make medicines safer by reporting suspected side effects: MHRA launches campaign

    • Published
    • Press release
    • MHRA
  4. Decide if your product is a medicine or a medical device

    • Updated
    • Detailed guide
    • MHRA
  5. Marketing authorisations: lists of granted licences

    • Updated
    • Collection
    • MHRA
  6. Marketing authorisations granted in October 2017

  7. Parallel import licences: lists of approved products

    • Updated
    • Collection
    • MHRA
  8. Parallel import licenses granted in October 2017

  9. E-cigarettes: regulations for consumer products

    • Updated
    • Detailed guide
    • MHRA
  10. Medicines: reclassify your product

  11. Conferences and events

    • Updated
    • Collection
    • MHRA
  12. The Yellow Card Scheme: guidance for healthcare professionals

    • Updated
    • Detailed guide
    • MHRA
  13. Human and veterinary medicines: register of licensed manufacturing sites 2017

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

  15. Medicines: new manufacturing and wholesale dealer licences

  16. Register of brokers authorised to deal in human medicines

  17. Human and veterinary medicines: register of licensed wholesale distribution sites

  18. Medicines: licensing time-based performance measures

    • Updated
    • Official Statistics
    • MHRA
  19. Review Panel Annual Report 2016

    • Published
    • Corporate report
    • MHRA
  20. Advisory Board on the Registration of Homeopathic Products and Herbal Medicines Advisory Committee Annual Reports 2016

    • Published
    • Corporate report
    • MHRA
  21. Make a payment to MHRA

    • Updated
    • Detailed guide
    • MHRA
  22. Drug Safety Update: monthly PDF newsletter

    • Updated
    • Guidance
    • MHRA
  23. Notify MHRA about a clinical investigation for a medical device

  24. Pharmacopoeial biological standards assure the quality of biological medicines

    • Published
    • News story
    • MHRA
  25. Strategy for pharmacopoeial public quality standards for biological medicines

    • Updated
    • Consultation outcome
    • MHRA
  26. MHRA phase I accreditation scheme

  27. Good manufacturing practice and good distribution practice

    • Updated
    • Detailed guide
    • DH and MHRA
  28. Register a homeopathic medicine or remedy

    • Updated
    • Detailed guide
    • MHRA
  29. Medicines: apply for a variation to your marketing authorisation

    • Updated
    • Detailed guide
    • MHRA
  30. South London man convicted for large number of unlicensed medicines

    • Published
    • Press release
    • MHRA
  31. Clinical trials for medicines: manage your authorisation, report safety issues

  32. Marketing authorisations granted in September 2017

  33. Parallel import licenses granted in September 2017

  34. Global health must survive political upheaval: Dr Jeremy Farrar delivers MHRA annual lecture

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

    • Updated
    • Detailed guide
    • MHRA
  36. Devices which incorporate an ancillary medicinal substance

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

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

    • Updated
    • Transparency data
    • MHRA
  39. Good laboratory practice (GLP) for safety tests on chemicals

    • Updated
    • Detailed guide
    • MHRA
  40. Early access to medicines scheme: expired scientific opinions

    • Updated
    • Decision
    • MHRA