Landmark endorsement of a global registry: The European Medicines Agency (EMA) Committee for Medicinal Products for Human Use (CHMP), publicly endorses World Federation of Hemophilia Gene Therapy Registry as global standard

Haemophilia. 2024 Jan;30(1):232-235. doi: 10.1111/hae.14912. Epub 2023 Dec 18.
No abstract available

Publication types

  • Letter

MeSH terms

  • Drug Approval
  • Europe
  • Hemophilia A* / drug therapy
  • Humans
  • Registries