RenuTend RSSAuthorisedThis medicine is authorised for use in the European Uniontenogenic primed equine allogeneic peripheral blood-derived mesenchymal stem cellsMedicineVeterinaryAuthorised
Page contentsOverviewProduct detailsAuthorisation detailsAssessment historyNews on RenuTendMore information on RenuTendApplication under evaluationCVMP opinionEuropean Commission decisionOverviewUp-to-date information on this veterinary medicinal product is available on the Veterinary Medicines Information websiteProduct details Name of medicine RenuTend Active substance tenogenic primed equine allogeneic peripheral blood-derived mesenchymal stem cells International non-proprietary name (INN) or common name tenogenic primed equine allogeneic peripheral blood-derived mesenchymal stem cells Pharmacotherapeutic groupMusculo-skeletal systemOther drugs for disorders of the musculo-skeletal systemAuthorisation details EMA product number EMEA/V/C/005428 Assessment historyInitial marketing authorisation documentsCVMP summary of positive opinion for RenuTendAdoptedReference Number: EMA/CVMP/73401/2022 English (EN) (131.59 KB - PDF)First published: 21/02/2022ViewNews on RenuTendMeeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 5-7 November 202408/11/2024Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 5-7 December 202308/12/2023Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 11-13 July 202314/07/2023Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 15-16 February 202221/02/2022More information on RenuTendArti-Cell Forte / RenuTend - direct healthcare professional communication (DHPC)This page was last updated on 21/02/2022Share this page