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Salesforce’s Agentforce Life Sciences Selected by AstraZeneca as Its Unified Global Platform to Help Transform Customer Engagement
SAN FRANCISCO--(BUSINESS WIRE)--Salesforce (NYSE: CRM), the world’s #1 CRM, today announced that AstraZeneca (LSE/STO/Nasdaq: AZN), a global, science-led biopharmaceutical company, has selected Agentforce Life Sciences for Customer Engagement to help transform its customer engagement globally, fostering stronger relationships with healthcare professionals (HCPs) through data-driven, AI-powered engagement. This work will support AstraZeneca's commitment to push the boundaries of science to deliv...
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Dietitian Live Announces Largest Real-World Reversal of Pre-Diabetes and Type 2 Diabetes Ever Recorded
MINNEAPOLIS--(BUSINESS WIRE)--Dietitian Live, a pioneering healthcare start-up that merges medical nutrition therapy with subconscious rewiring to reverse chronic disease, today announced a healthcare breakthrough showing that the human brain is the primary driver of healing in chronic metabolic disease. Through its patent-pending Quantum Mind Architecture™ program, the company has demonstrated that when subconscious beliefs are rewired from fear to love, the body’s biology naturally realigns w...
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Listening to Healthcare Professionals: Dexcom Launches New Education Offering, Dexcom Academy
EDINBURGH, Scotland--(BUSINESS WIRE)--DexCom, Inc. (NASDAQ:DXCM), a global leader in real-time continuous glucose monitoring (CGM) for people with diabetes, today announced the launch of Dexcom Academy, a new personalised learning platform created with healthcare professionals (HCPs) and for healthcare professionals. The platform is now available in Belgium, Germany, the Kingdom of Saudi Arabia, the Netherlands, and Spain with further EMEA country launches planned for 2026. Guided directly by H...
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Insulet Announces FDA 510(k) Clearance of Omnipod® 5 Algorithm Enhancements that Redefine Insulin Delivery and Simplify the Pod Experience
ACTON, Mass.--(BUSINESS WIRE)--Insulet Corporation (NASDAQ: PODD) (Insulet or the Company), the global leader in tubeless insulin pump technology with its Omnipod® brand of products, today announced it has received FDA 510(k) clearance for significant enhancements to the Omnipod 5 Automated Insulin Delivery System. These updates to the Omnipod 5 algorithm set a new benchmark in tubeless diabetes technology by offering a lower 100 mg/dL Target Glucose option and a more seamless automated experie...
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Junevity Expands Seed Funding to $20 Million for Cell Reprogramming with siRNA
SAN FRANCISCO--(BUSINESS WIRE)--Junevity Expands Seed Funding to $20 Million for Cell Reprogramming with siRNA...
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Vorgefüllte Spritze BYOOVIZ® von Samsung Bioepis, das Biosimilar zu Lucentis (Ranibizumab), erhält europäische Zulassung
INCHEON, Korea--(BUSINESS WIRE)--Samsung Bioepis Co., Ltd. gab heute bekannt, dass der Ausschuss für Humanarzneimittel (CHMP) der Europäischen Arzneimittelagentur (EMA) eine positive Stellungnahme zu BYOOVIZ® Fertigspritzen (PFS) abgegeben hat, einem Biosimilar, das sich auf Lucentis1 (Ranibizumab) bezieht. BYOOVIZ wurde erstmals im August 2021 von der Europäischen Kommission (EK) als Einwegampulle zur intravitrealen Anwendung (0,5 mg/0,05 ml) für die Behandlung der neovaskulären (feuchten) alt...
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La présentation en seringue préremplie de BYOOVIZ®, le médicament biosimilaire de Lucentis (ranibizumab) de Samsung Bioepis, obtient l’autorisation européenne
INCHEON, Corée--(BUSINESS WIRE)--Samsung Bioepis Co., Ltd. a annoncé aujourd’hui que le Comité des médicaments à usage humain (CHMP) de l’Agence européenne des médicaments (EMA) a rendu un avis favorable concernant la seringue préremplie (PFS) BYOOVIZ®, un médicament biosimilaire de référence Lucentis1 (ranibizumab). BYOOVIZ a été approuvé pour la première fois par la Commission européenne (CE) en août 2021 en tant que flacon à usage unique pour administration intravitréenne (0,5 mg/0,05 ml) da...
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Resumen: La jeringa precargada BYOOVIZ®, el biosimilar de Lucentis (ranibizumab) de Samsung Bioepis, obtiene la aprobación de Europa
INCHEON, Corea--(BUSINESS WIRE)--Samsung Bioepis Co., Ltd. ha anunciado hoy que el Comité de Medicamentos de Uso Humano (CHMP) de la Agencia Europea de Medicamentos (EMA) ha emitido un dictamen favorable para la jeringa precargada (PFS) de BYOOVIZ®, un biosimilar de referencia de Lucentis1 (ranibizumab). El comunicado en el idioma original es la versión oficial y autorizada del mismo. Esta traducción es solamente un medio de ayuda y deberá ser comparada con el texto en idioma original, que es l...
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Riassunto: La presentazione della siringa preriempita di BYOOVIZ®, il biosimilare di Lucentis (ranibizumab) di Samsung Bioepis, ottiene l'approvazione europea
INCHEON, Corea--(BUSINESS WIRE)--Samsung Bioepis Co., Ltd. ha annunciato oggi che il Comitato per i medicinali per uso umano (CHMP) dell'Agenzia europea per i medicinali (EMA) ha adottato un'opinione positiva per la siringa pre-riempita (PFS) di BYOOVIZ®, un biosimilare che ha come farmaco di riferimento Lucentis1 (ranibizumab). Il testo originale del presente annuncio, redatto nella lingua di partenza, è la versione ufficiale che fa fede. Le traduzioni sono offerte unicamente per comodità del...
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Samenvatting: Voorstelling van voorgevulde spuit BYOOVIZ®, de biosimilar van Samsung Bioepis voor Lucentis (ranibizumab), krijgt Europese goedkeuring
INCHEON, Korea--(BUSINESS WIRE)--Samsung Bioepis Co., Ltd. maakte vandaag bekend dat de CHMP (Committee for Medicinal Products for Human Use) van EMA (European Medicines Agency) een positief advies geeft voor de voorgevulde spuit (PFS) BYOOVIZ®, een biosimilar die refereert naar Lucentis1 (ranibizumab). Deze bekendmaking is officieel geldend in de originele brontaal. Vertalingen zijn slechts als leeshulp bedoeld en moeten worden vergeleken met de tekst in de brontaal, die als enige rechtsgeldig...
