Newsroom | 70616 results

COCOA BEACH, Fla. & MOORESVILLE, N.C.--(BUSINESS WIRE)--Alesis LLC, the U.S. distributor of the Alesis OSA1™ medical device and headquartered on Florida’s Space Coast in Cocoa Beach, today announced a joint venture partnership with Lake Norman Pulmonary & Sleep in Mooresville, North Carolina — making it the first sleep medicine practice in the Piedmont region to offer Alesis OSA1, a breakthrough non-surgical treatment for patients with obstructive sleep apnea (OSA) who cannot tolerate CPAP...

HYOGO, Japan--(BUSINESS WIRE)--JCR will present preclinical data from its novel platform technologies, including JUST-AAV gene therapy, at the ASGCT 29th Annual Meeting this week....

BROOMALL, Pa.--(BUSINESS WIRE)--Drummond Scientific Company today announced the acquisition of Accu-Glass, LLC, a St. Louis-based manufacturer of high-precision glass capillaries....

MEMPHIS, Tenn.--(BUSINESS WIRE)--St. Jude Children’s Research Hospital® hosted more than 60 teenage patients and their guests for the 2026 St. Jude Teen Formal at the Domino’s Event Center on campus. Teen Formal is one of several thoughtfully designed experiences created by St. Jude to honor meaningful milestones in patients’ lives—moments they might otherwise miss while undergoing treatment for cancer or other life‑threatening diseases. This year’s event was themed “On Cloud 9,” inspired by St...

比利時根特和東京--(BUSINESS WIRE)--(美國商業資訊)-- H.U. Group Holdings Inc.及其獨資子公司Fujirebio今日宣布，Fujirebio Europe N.V.已依據《歐盟(EU) 2017/746體外診斷醫療器材法規》(IVDR)取得Lumipulse G pTau 217血漿檢測試劑盒的CE認證。該化學發光酵素免疫分析(CLEIA)檢測可對人體血漿(K2 EDTA)中的蘇胺酸217磷酸化Tau蛋白(pTau 217)進行量化檢測。 Fujirebio Europe N.V.執行長Christiaan De Wilde表示：「隨著Lumipulse G NfL血液檢測和Lumipulse G pTau 217血漿檢測均在我們的LUMIPULSE G平台完成CE認證，我們正邁入神經診斷的全新時代——憑藉血液生物標記，能夠更早、更廣泛、更便捷地洞察阿茲海默症和神經退化性病變。透過提供全自動和可擴充的解決方案，我們協助臨床醫師更果斷地做出更及時、更明智的決策。這一里程碑印證了我們的長期願景：重塑診斷路徑，並透過創新、精準與合作，從根本上改善歐...

比利时根特和东京--(BUSINESS WIRE)--(美国商业资讯)-- H.U. Group Holdings Inc.及其全资子公司Fujirebio今日宣布，Fujirebio Europe N.V.已依据《欧盟(EU) 2017/746体外诊断医疗器械法规》(IVDR)取得Lumipulse G pTau 217血浆检测试剂盒的CE认证。该化学发光酶免疫分析(CLEIA)检测可对人体血浆(K2 EDTA)中的苏氨酸217磷酸化Tau蛋白(pTau 217)进行定量检测。 Fujirebio Europe N.V.首席执行官Christiaan De Wilde表示：“随着Lumipulse G NfL血液检测和Lumipulse G pTau 217血浆检测均在我们的LUMIPULSE G平台完成CE认证，我们正迈入神经诊断的全新时代——依托血液生物标志物，能够更早、更广泛、更便捷地洞察阿尔茨海默病和神经退行性病变。通过提供全自动和可扩展的解决方案，我们助力临床医师更果断地做出更及时、更明智的决策。这一里程碑印证了我们的长期愿景：重塑诊断路径，并通过创新、精准与合作，从根本上...

GENT, België & TOKIO--(BUSINESS WIRE)--H.U. Group Holdings Inc. en haar volledige dochteronderneming Fujirebio hebben vandaag bekendgemaakt dat Fujirebio Europe N.V. een CE-certificaat heeft verkregen voor de Lumipulse G pTau 217 Plasma-test op grond van Verordening (EU) 2017/746 betreffende in vitro in vitro diagnostische medische hulpmiddelen (IVDR). Deze CLEIA-test (chemiluminescente enzymimmunoassay) maakt de kwantitatieve meting mogelijk van tau gefosforyleerd op threonine 217 (pTau 217) i...

GAND, Belgio, e TOKYO--(BUSINESS WIRE)--H.U. Group Holdings Inc. e la sua controllata al 100% Fujirebio oggi hanno reso noto che Fujirebio Europe N.V. ha ottenuto la certificazione CE per il saggio Lumipulse G pTau 217 Plasma nel quadro del Regolamento (UE) 2017/746 sui dispositivi medico-diagnostici in vitro(IVDR). Questo immunodosaggio enzimatico in chemiluminescenza (CLEIA) consente di quantificare la proteina Tau fosforilata sulla treonina 217 (pTau 217) nel plasma umano (K2 EDTA). "L'otten...

GHENT, Bélgica & TÓQUIO--(BUSINESS WIRE)--A H.U. Group Holdings Inc. e sua subsidiária integral Fujirebio anunciaram hoje que a Fujirebio Europe N.V. obteve o certificado CE para o ensaio Lumipulse G pTau 217 Plasma, nos termos do Regulamento (UE) 2017/746 relativo aos dispositivos médicos para diagnóstico in vitro (IVDR). Este teste CLEIA (imunoensaio enzimático quimioluminescente) permite a medição quantitativa da proteína Tau fosforilada na treonina 217 (pTau 217) no plasma humano (2 EDTA)....

GENT, Belgien & TOKIO--(BUSINESS WIRE)--Die H.U. Group Holdings Inc. und ihre hundertprozentige Tochtergesellschaft Fujirebio gaben heute bekannt, dass Fujirebio Europe N.V. ein CE-Zertifikat für den Lumipulse G pTau 217 Plasma-Assay gemäß der Verordnung (EU) 2017/746 über In-vitro -Diagnostika (IVDR) erhalten hat. Dieser CLEIA-Test (Chemilumineszenz-Enzymimmunoassay) ermöglicht die quantitative Bestimmung von an Threonin 217 phosphoryliertem Tau (pTau 217) in humanem Plasma (K2 EDTA). „Mit den...