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    "fda" โ€” Press Releases

    8,255 releases found

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    ๐Ÿ“‹ Business ๐Ÿ“ฃ PR News
    Veristat Supported Marketing Applications for 12% of all FDA Novel Drug Approvals in 2021. SOUTHBOROUGH, Mass., MA-VERISTAT
    Expertini PR News  ยท  1604 days ago
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    Les instances rรฉglementaires autorisent la pompe Impella 5.5 avec SmartAssist au Japon et ร  Hong Kong au moment oรน la FDA amรฉricaine octroie une dispense conditionnelle de dispositif expรฉrimental ร  Impella BTR dans le cadre de la premiรจre รฉtude de.... DANVERS, Massachusetts, MA-ABIOMED
    Expertini PR News  ยท  1604 days ago
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    CARsgen Announces CT041 CAR T-cell Product Candidate Granted RMAT Designation by the FDA
    Expertini PR News  ยท  1605 days ago
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    AbbVie Submits Applications for Upadacitinib (RINVOQยฎ) in Non-Radiographic Axial Spondyloarthritis to U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA)
    Expertini PR News  ยท  1608 days ago
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    BIOLASE and EdgeEndo Announce FDA 510(k) Clearance of New EdgePRO Laser-Assisted Microfluidic Irrigation Device for Endodontists
    Expertini PR News  ยท  1609 days ago
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    ๐Ÿ“‹ Health ๐Ÿ“ฃ PR News
    REGENXBIO Announces FDA Clearance of IND for Clinical Trial of RGX-202, a Novel Gene Therapy Candidate for Duchenne Muscular Dystrophy
    Expertini PR News  ยท  1609 days ago
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    ๐Ÿ“‹ Business ๐Ÿ“ฃ PR News
    Avcon Caravan Aircraft Sensor Platform FAA STC Approved
    Expertini PR News  ยท  1610 days ago
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    ProcessMAP Partners With Hg, a Global Software Investor, to Accelerate Its Strategy Towards Becoming a Global Software Leader in Worker Health and Safety Management. FT. LAUDERDALE, Fla. & NEW YORK, NY-HG
    Expertini PR News  ยท  1610 days ago
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    ANANDA Scientific Announces FDA approval of the IND for the Clinical Trial on the Treatment of Opioid Use Disorder (OUD). GREENWOOD VILLAGE, Colo. & LOS ANGELES, CO-ANANDA-SCIENTIFIC
    Expertini PR News  ยท  1611 days ago
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    Best's Commentary: Brand Profile and Pricing Models in Focus as UK Insurers Adjust to New FCA Rules. LONDON, AM-BEST
    Expertini PR News  ยท  1611 days ago
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    Everest Medicines Announces Taiwan FDA Has Accepted New Drug Application for Sacituzumab Govitecan in Second-Line Metastatic Triple-Negative Breast Cancer
    Expertini PR News  ยท  1612 days ago
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    ๐Ÿ“‹ Business ๐Ÿ“ฃ PR News
    Zynex Submits FDA Application for its Next Generation Fluid and Blood Volume Monitor
    Expertini PR News  ยท  1612 days ago
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    Novavax Submits Final Data Packages to U.S. FDA as Prerequisite to Emergency Use Authorization Application Request for COVID-19 Vaccine
    Expertini PR News  ยท  1615 days ago
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    ๐Ÿ“‹ Business ๐Ÿ“ฃ PR News
    A LEO Pharma bejelentette, hogy a kรถzรฉpsรบlyos-sรบlyos atรณpiรกs dermatitiszben szenvedล‘ felnล‘ttek kezelรฉsรฉre szolgรกlรณ, specifikusan az IL-13-at cรฉlzรณ Adbryโ„ข (tralokinumab) elsล‘ รฉs ez idรกig egyetlen ilyen kรฉszรญtmรฉnykรฉnt megkapta az FDA jรณvรกhagyรกsรกt. BALLERUP, Dรกnia, LEO-PHARMA
    Expertini PR News  ยท  1617 days ago
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    LEO Pharma anuncia a aprovaรงรฃo pelo FDA do Adbryโ„ข (tralocinumab) como o primeiro e รบnico tratamento direcionado especificamente ร  IL-13 para adultos com dermatite atรณpica moderada a grave. BALLERUP, Dinamarca, LEO-PHARMA
    Expertini PR News  ยท  1617 days ago
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    LEO Pharma annuncia l'approvazione per Adbryโ„ข (tralokinumab) da parte della FDA, come primo e unico trattamento mirato specificamente all'IL-13 per gli adulti con dermatite atopica da moderata a grave. BALLERUP, Danimarca, LEO-PHARMA
    Expertini PR News  ยท  1618 days ago
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    LEO Pharma anuncia que la FDA ha aprobado Adbryโ„ข (tralokinumab) como el primer y รบnico tratamiento dirigido especรญficamente a la IL-13 para adultos con dermatitis atรณpica de moderada a grave. BALLERUP, Dinamarca, LEO-PHARMA
    Expertini PR News  ยท  1618 days ago
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    ๐Ÿ“‹ Business ๐Ÿ“ฃ PR News
    LEO Pharma Announces FDA Approval of Adbryโ„ข (tralokinumab) as the First and Only Treatment Specifically Targeting IL-13 for Adults With Moderate-to-Severe Atopic Dermatitis. BALLERUP, Denmark, LEO-PHARMA
    Expertini PR News  ยท  1618 days ago
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    ๐Ÿ“‹ Business ๐Ÿ“ฃ PR News
    Aimmuneโ€™s PALFORZIAยฎโ–ผ [defatted powder of Arachis hypogaea L., semen (peanuts)] Receives Final Appraisal Determination (FAD) as Positive Draft Guidance From NICE for the Treatment of Peanut Allergy in Patients Aged 4 to 17 Years. LONDON, AIMMUNE-THERAPEUTICS-UK
    Expertini PR News  ยท  1623 days ago
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    Takeda Recebe Carta de Resposta Completa do FDA dos EUA para TAK-721. OSAKA, Japรฃo & CAMBRIDGE, Mass., MA-TAKEDA-PHARMACEUTICAL
    Expertini PR News  ยท  1624 days ago
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