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Aicuris Appoints Jacques Dumas as Chief Scientific Officer

WUPPERTAL, Germany–(BUSINESS WIRE)–Aicuris announced today the appointment of Jacques Dumas, Ph.D., as Chief Scientific Officer (CSO), effective January 1, 2025. Dr. Dumas brings over 30 years of experience in pharmaceutical research and development (R&D), with a strong track record of advancing innovative medicines in oncology and infectious diseases from the discovery to launch. In his new role, Dr. Dumas will oversee Aicuris’ R&D efforts, ensuring alignment with the company’s strat
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Research Using Mirvie RNA Platform Selected for Plenary Session Presentation at the Society for Maternal and Fetal Medicine Annual Meeting

SOUTH SAN FRANCISCO, Calif.–(BUSINESS WIRE)–Mirvie, a company bringing a personalized, predictive, and preventive approach to pregnancy complications, today announced the company was selected to present new research demonstrating the ability of the Mirvie RNA platform to predict the risk of severe fetal growth restriction in pregnancy. The abstract, “Prediction of severely small-for-gestational-age infants using a novel cell-free RNA model,” will be presented on Thursday, January 30, 2025 9:1
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Azafaros granted important regulatory designations and clearance by European authorities for global Phase 3 studies, to be initiated in 2025

LEIDEN, Netherlands–(BUSINESS WIRE)– #Adults–Azafaros B.V. today announced that its lead asset, nizubaglustat, has been granted orphan drug designation from regulatory authorities in both the United States and the European Union for the treatment of GM1 gangliosidosis. Additionally, the company’s Clinical Trial Application (CTA) for two global Phase 3 studies investigating the drug’s efficacy and safety in GM1/GM2 gangliosidoses and Niemann-Pick Type C (NPC) was approved by multiple European countries
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Parse Biosciences cuadruplica las capacidades de multiplexación de muestras de los kits Evercode WT Mega

SEATTLE–(BUSINESS WIRE)–Parse Biosciences, líder en soluciones de secuenciación unicelular accesibles y escalables, acaba de anunciar una importante ampliación de la funcionalidad de su kit Evercode™ WT Mega. Los investigadores ahora pueden analizar hasta 384 muestras y 1 millón de células en un solo ciclo, lo que abre nuevas posibilidades para estudios de alto rendimiento. Aunque las tecnologías de secuenciación unicelular no han dejado de avanzar, muchas de ellas siguen teniendo limitacione
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Aiosyn Mitosis Breast devient la première solution de détection des mitoses basée sur l'IA à obtenir la certification du marquage CE dans le cadre de l'IVDR.

NIJMEGEN, Pays-Bas–(BUSINESS WIRE)–Aiosyn, un innovateur pionnier dans le domaine des logiciels de pathologie basés sur l’IA pour le cancer et les maladies rénales, a annoncé que son algorithme de comptage des figures mitotiques a obtenu le marquage CE dans le cadre du règlement sur les dispositifs médicaux de diagnostic in vitro (IVDR) en vue d’une utilisation dans le domaine du diagnostic. Cette étape établit Aiosyn Mitosis Breast comme la première application certifiée IVDR pour le comptag
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Parse Biosciences quadruplica a capacidade de multiplexação de amostras dos Evercode WT Mega Kits

SEATTLE–(BUSINESS WIRE)–A Parse Biosciences, líder em soluções acessíveis e escalonáveis para sequenciamento de células individuais, anunciou hoje uma expansão significativa na funcionalidade do Evercode™ WT Mega Kit. Agora, os pesquisadores podem analisar até 384 amostras e 1 milhão de células em um único experimento, abrindo novas possibilidades para estudos de alto rendimento. Embora as tecnologias de células individuais tenham avançado constantemente, muitas ainda enfrentam limitações ao
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Aiosyn Mitosis Breast ist die erste KI-gestützte Lösung zur Mitoseerkennung, die die CE-Zertifizierung gemäß IVDR erhält

NIJMEGEN, Niederlande–(BUSINESS WIRE)–Aiosyn, ein Pionier im Bereich KI-gestützter Pathologiesoftware für Krebs- und Nierenerkrankungen, hat bekannt gegeben, dass sein Algorithmus zur Zählung mitotischer Figuren die CE-Kennzeichnung gemäß der In-Vitro-Diagnostik-Verordnung (IVDR) für den Einsatz in der Diagnostik erhalten hat. Dieser Meilenstein etabliert Aiosyn Mitosis Breast als erste IVDR-zertifizierte Anwendung für die Mitosenzählung in der Brustkrebsdiagnostik und beschleunigt das Wachst
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Aiosyn Mitosis Breast wordt de eerste AI-oplossing voor mitose-detectie die CE-markering krijgt onder IVDR

NIJMEGEN, Nederland–(BUSINESS WIRE)–Aiosyn, een baanbrekende vernieuwer in AI-aangedreven pathologiesoftware voor kanker en nieraandoeningen, heeft aangekondigd dat zijn algoritme voor het tellen van mitotische figuren CE-markering heeft gekregen onder de In Vitro Diagnostic Regulation (IVDR) voor gebruik in de diagnostiek. Deze mijlpaal bevestigt Aiosyn Mitosis Breast als de eerste IVDR-gecertificeerde toepassing voor mitosetelling in borstkankerdiagnose en versnelt de groei van het bedrijf
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Aiosyn Mitosis Breast diventa la prima soluzione di rilevamento della mitosi alimentata dall'IA per ottenere la certificazione CE ai sensi dell'IVDR

NIJMEGEN, Paesi Bassi–(BUSINESS WIRE)–Aiosyn, un pioniere nell’innovazione del software per patologie oncologiche e renali alimentato dall’IA, ha annunciato che il suo algoritmo per la conta mitotica ha ottenuto il marchio CE nell’ambito del regolamento per la diagnostica in vitro (IVDR) per l’uso in diagnostica. Questo traguardo rende Aiosyn Mitosis Breast la prima applicazione certificata IVDR per la conta mitotica nella diagnostica del tumore al seno e accelera l’espansione dell’azienda ne
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