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"fda" โ Press Releases
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Senhwa's Silmitasertib Receives US FDA Orphan Drug Designation for the Treatment of Medulloblastoma
Publisher ยท 2021
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300,000-Patient Primary Care Network in Canada Achieves Substantial Savings with UKG. LOWELL, Mass. & WESTON, Fla., UKG
Publisher ยท 2021
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Perimeter Medical Imaging AI Announces Important Milestone in ATLAS AI Project With FDA Investigational Device Exemption (IDE) Approval to Launch Clinical Trial Using Perimeter B-Series OCT With ImgAssist AI in Breast Conservation Surgery. TORONTO & DALLAS, TX-PERIMETER-MEDICAL
Publisher ยท 2021
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Pentwater Issues Open Letter to Turquoise Hill Demanding Transparency and Accountability. NAPLES, Fla., FL-PENTWATER-CAPITAL
Publisher ยท 2021
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Gan and Lee Pharmaceuticals Announces U.S. FDA Clearance of Investigational New Drug (IND) Application for a Novel Glucagon-Like Peptide-1 Analogue, GZR18
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Gan & Lee Pharmaceuticals Announces U.S. FDA Clearance of Investigational New Drug (IND) Application for a Novel Glucagon-Like Peptide-1 Analogue, GZR18
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Caldera Medical Announces FDA Clearance for New Desaraยฎ TVez for Stress Urinary Incontinence. LOS ANGELES, CA-CALDERA-MEDICAL
Publisher ยท 2021
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Caldera Medical anuncia autorizaรงรฃo da FDA para novo Desaraยฎ TVez para incontinรชncia urinรกria de esforรงo. LOS ANGELES, CA-CALDERA-MEDICAL
Publisher ยท 2021
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DigitalBridge Anuncia Investimento da IFC para Aprimorar Infraestrutura Digital e Conectividade na Amรฉrica Latina e no Sudeste Asiรกtico. BOCA RATรN, Fla., FL-DIGITALBRIDGE
Publisher ยท 2021
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QIAGEN und DiaSorin erweitern Zugang zu Tests auf latente TB in den USA mit FDA-Zulassung des QuantiFERONยฎ-TB Gold Plus Tests fรผr LIAISONยฎ-XS-Plattformen. HILDEN, Deutschland & SALUGGIA, Italien, QIAGEN
Publisher ยท 2021
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The Great EDA Migration: 85% of businesses striving for Event-Driven Architecture
Publisher ยท 2021
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Treadwell Therapeutics Announces US FDA Clearance of IND Application for Phase 2 Study of TTK inhibitor, CFI-402257
Publisher ยท 2021
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Lunit's AI Software for Breast Cancer Detection, Lunit INSIGHT MMG, Wins FDA Clearance
Publisher ยท 2021
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Isofol Medical AB (publ) will not reach 300 PFS events in the AGENT study with current censoring rules based on FDA decision
Publisher ยท 2021
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ๆฐๆ็งๆๅฎๆดEDAๆต็จ็ๅ ่ทๅพไธๆ4LPPๅทฅ่บ่ฎค่ฏ
Publisher ยท 2021
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Moleculin Receives FDA Allowance to Begin a Phase 1 Study of WP1122 for the Treatment of Glioblastoma Multiforme
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U.S. FDA Grants Bionomics Fast Track Designation to BNC210 for the Acute Treatment of Social Anxiety Disorder and Other Anxiety Related Disorders
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The Great EDA Migration: 85% of businesses striving for Event-Driven Architecture
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Evofem Biosciences Announces Successful Type C Meeting with FDA for STI Prevention Product Candidate
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RegeneRx Joint Venture Requests Pre-BLA Meeting with FDA For RGN-259 for Dry Eye Syndrome
Publisher ยท 2021
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