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La Commissione europea (CE) approva BILDYOS® (denosumab) e BILPREVDA® (denosumab) di Henlius e Organon, biosimilari rispettivamente di PROLIA (denosumab) e XGEVA (denosumab)
SHANGHAI e JERSEY CITY, N.J.--(BUSINESS WIRE)--Shanghai Henlius Biotech, Inc. (2696.HK), e Organon (NYSE: OGN) oggi hanno annunciato che la Commissione europea (CE) ha concesso l'autorizzazione all'immissione in commercio di BILDYOS® (denosumab) soluzione iniettabile da 60 mg/ml e BILPREVDA® (denosumab) soluzione iniettabile da 120 mg/1,7 ml, biosimilari rispettivamente di PROLIA (denosumab) e XGEVA (denosumab), per tutte le indicazioni dei prodotti di riferimento.1,2 “Le autorizzazioni di BILD...
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Europese Commissie (EC) keurt BILDYOS® (denosumab) en BILPREVDA® (denosumab) van Henlius en Organon goed, biosimilars van respectievelijk PROLIA (denosumab) en XGEVA (denosumab)
SHANGHAI & JERSEY CITY, N.J.--(BUSINESS WIRE)--Shanghai Henlius Biotech, Inc. (2696, HK) en Organon (NYSE: OGN) hebben vandaag aangekondigd dat de Europese Commissie (EC) een handelsvergunning heeft verleend voor BILDYOS® (denosumab)-injectie 60 mg/ml en BILPREVDA® (denosumab)-injectie 120 mg/1,7 ml, biosimilars van respectievelijk PROLIA (denosumab) en XGEVA (denosumab), voor alle indicaties van de referentieproducten.1,2 "De goedkeuringen door de EC van BILDYOS en BILPREVDA markeren een cruci...
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La Commission européenne (CE) approuve BILDYOS® (denosumab) et BILPREVDA® (denosumab) de Henlius et Organon, biosimilaires respectivement de PROLIA (denosumab) et XGEVA (denosumab)
SHANGHAI et JERSEY CITY, New Jersey--(BUSINESS WIRE)--Shanghai Henlius Biotech, Inc. (2696.HK) et Organon (NYSE : OGN) ont annoncé aujourd’hui que la Commission européenne (CE) avait accordé une autorisation de mise sur le marché pour BILDYOS® (denosumab) injection 60 mg/mL et BILPREVDA® (denosumab) injection 120 mg/1,7 mL, biosimilaires de PROLIA (denosumab) et XGEVA (denosumab), respectivement, pour toutes les indications des produits de référence.1,2 « Les autorisations de mise sur le marché...
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La Comisión Europea (CE) aprueba BILDYOS® (denosumab) y BILPREVDA® (denosumab) de Henlius y Organon, biosimilares de PROLIA (denosumab) y XGEVA (denosumab), respectivamente
SHANGHAI y JERSEY CITY, Nueva Jersey--(BUSINESS WIRE)--Shanghai Henlius Biotech, Inc. (2696.HK) y Organon (NYSE: OGN) acaban de anunciar que la Comisión Europea (CE) ha autorizado la comercialización de BILDYOS® (denosumab) inyectable 60 mg/ml y BILPREVDA® (denosumab) inyectable 120 mg/1,7 ml, biosimilares de PROLIA (denosumab) y XGEVA (denosumab), respectivamente, para todas las indicaciones de los productos de referencia.1,2 «Las aprobaciones de la CE de BILDYOS y BILPREVDA suponen un hito cr...
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Die Europäische Kommission (EK) genehmigt BILDYOS® (Denosumab) von Henlius und Organon sowie BILPREVDA® (Denosumab), Biosimilars zu PROLIA (Denosumab) bzw. XGEVA (Denosumab)
SHANGHAI UND JERSEY CITY, NEW JERSEY--(BUSINESS WIRE)--Shanghai Henlius Biotech, Inc. (2696.HK) und Organon (NYSE: OGN) gaben heute die Erteilung der Marktzulassung durch die Europäische Kommission (EK) für die BILDYOS® (Denosumab)-Injektion 60 mg/ml und die BILPREVDA® (Denosumab)-Injektion 120 mg/1,7 ml bekannt, Biosimilars zu PROLIA (Denosumab) bzw. XGEVA (Denosumab. Diese Zulassung gilt für alle Indikationen der Referenzprodukte.1,2 „Die Zulassung von BILDYOS und BILPREVDA durch die EK ist e...
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Tanner Health and Healthliant Ventures Partner with Incision USA on Innovative OR Solutions
CARROLLTON, Ga.--(BUSINESS WIRE)--Tanner Health and Healthliant Ventures are pleased to announce a partnership with Incision USA, a healthcare technology company dedicated to supporting surgical teams with intuitive, clinician-designed tools that foster confidence, well-being and efficiency. With Incision’s Assist and Academy solutions, operating room (OR) staff can confidently prepare for surgical cases by giving them on-demand access to surgeon preferences, team workflows, visual OR setup gui...
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Asia-Pacific Stereotactic Neuro-Navigation System Research and Forecast Report 2025-2035 | Competitive Analysis of Saphirex Surgicals, SURGLASSES, and HRS Navigation - ResearchAndMarkets.com
DUBLIN--(BUSINESS WIRE)--The "Asia-Pacific Stereotactic Neuro-Navigation System Market: Analysis and Forecast, 2025-2035" report has been added to ResearchAndMarkets.com's offering. The Asia-Pacific stereotactic neuro-navigation system market is projected to reach $702.2 million by 2035 from $170.7 million in 2024, growing at a CAGR of 14.05% during the forecast period 2025-2035. The market for APAC stereotactic neuro-navigation systems is expanding quickly due to the increased prevalence of ne...
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Europe Stereotactic Neuro-Navigation System Market Report 2025-2035 | Opportunities Fueled by Integration of Artificial Intelligence (AI) and Machine Learning - ResearchAndMarkets.com
DUBLIN--(BUSINESS WIRE)--The "Europe Stereotactic Neuro-Navigation System Market: Analysis and Forecast, 2025-2035" report has been added to ResearchAndMarkets.com's offering. The Europe stereotactic neuro-navigation system market is projected to reach $1.01 billion by 2035 from $269.0 million in 2024, growing at a CAGR of 13.14% during the forecast period 2025-2035. The market for stereotactic neuro-navigation systems in Europe is expected to develop significantly due to the rising demand for...
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Asia-Pacific Robotic Neurosurgery Research and Forecast Report 2025-2035 | Rapid Expansion Fueled by Healthcare Infrastructure Throughout Emerging APAC Markets - ResearchAndMarkets.com
DUBLIN--(BUSINESS WIRE)--The "Asia-Pacific Robotic Neurosurgery Market: Analysis and Forecast, 2025-2035" report has been added to ResearchAndMarkets.com's offering. The Asia-Pacific robotic neurosurgery market is projected to reach $587.0 million in 2035 and estimated $92.6 million in 2025, growing at a CAGR of 20.28% during the forecast period 2025-2035 The increasing popularity of minimally invasive procedures is speeding up adoption even more because they lower surgical risks and recuperati...
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European Commission (EC) Approves Henlius and Organon’s BILDYOS® (denosumab) and BILPREVDA® (denosumab), Biosimilars to PROLIA (denosumab) and XGEVA (denosumab), Respectively
SHANGHAI & JERSEY CITY, N.J.--(BUSINESS WIRE)--European Commission Approves Henlius and Organon’s BILDYOS® (denosumab) and BILPREVDA® (denosumab), Biosimilars......