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UK's Medicines Regulator Announces Guidance on the New International Recognition Procedure for the Approval of New Medicines from 1 January 2024 | Goodwin

Earlier this year, the UK’s medicines regulator, the Medicines and Healthcare products Regulatory Agency (MHRA), announced that a new International Recognition Procedure (IRP) will be...
United States United Kingdom Great Britain European Commission Decision Reliance Procedure European Union Committee For Medicinal Products Human

Vertex Pharmaceuticals Incorporated Receives Chmp Positive Opinion for Kaftrio® (Ivacaftor/Tezacaftor/Elexacaftor) in Combination with Ivacaftor for Children with Cystic Fibrosis Ages 2 Through 5

Vertex Pharmaceuticals Incorporated announced that the European Medicines Agency?s Committee for Medicinal Products for Human Use adopted a positive opinion for the label extension of KAFTRIO® in...
European Union European Medicines Agency Vertex Pharmaceuticals Incorporated Committee For Medicinal Products Human Use European Medicines Medicinal Products

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