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Recordati Rare Diseases verkündet die Veröffentlichung der Langzeitergebnisse der Verlängerung der Phase-III-Studie LINC 3 zu Isturisa® (Osilodrostat) in Patienten mit Cushing’s Syndrom im European Journal of Endocrinology: https://mms.businesswire.com/media/20200601005592/en/794449/5/RRD_LOGO_tagline_TM-CMYK_Black_highres.jpg
Recordati Rare Diseases verkündet die Veröffentlichung der Langzeitergebnisse der Verlängerung der Phase-III-Studie LINC 3 zu Isturisa® (Osilodrostat) in Patienten mit Cushing’s Syndrom im European Journal of Endocrinology


Recordati Rare Diseases gab heute die Veröffentlichung der Langzeitergebnisse der offenen Verlängerungsphase der Phase-III-Studie LINC 3 mit Isturisa® im European Journal of Endocrinology bekannt.1

Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
DGAP-News: BB BIOTECH AG: Moderna was just the beginning
DGAP-News: BB BIOTECH AG: Moderna was just the beginning
DGAP-News: BB BIOTECH AG: Moderna was just the beginning
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Charles River Laboratories Expands Contract Vivarium Space on West Coast: https://mms.businesswire.com/media/20191106005189/en/754630/5/charles_river_logo.jpg
Charles River Laboratories Expands Contract Vivarium Space on West Coast


Charles River Laboratories International, Inc. (NYSE: CRL) today announced the addition of five Charles River Accelerator and Development Lab (CRADL™) locations in California and Washington. CRADL

Sonova to enable fully immersive conversations in virtually any situation with new Lumity platform
Sonova to enable fully immersive conversations in virtually any situation with new Lumity platform
Sonova to enable fully immersive conversations in virtually any situation with new Lumity platform
CSL Vifor and Travere Therapeutics announce EMA has accepted for review the Conditional Marketing Authorization application for sparsentan for the treatment of IgA Nephropathy: https://mms.businesswire.com/media/20191103005014/en/691947/5/VP_logo_rgb.jpg
CSL Vifor and Travere Therapeutics announce EMA has accepted for review the Conditional Marketing Authorization application for sparsentan for the treatment of IgA Nephropathy


CSL Vifor and Travere Therapeutics, Inc. (NASDAQ: TVTX) today announced that the EMA has accepted for review the Conditional Marketing Authorization (CMA) application for sparsentan for the

Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
VFMCRP announces U.S. Court upholds validity of Velphoro® patent: https://mms.businesswire.com/media/20191103005014/en/691947/5/VP_logo_rgb.jpg
VFMCRP announces U.S. Court upholds validity of Velphoro® patent


Vifor Fresenius Medical Care Renal Pharma (VFMCRP) today announced that the U.S. District Court for the District of Delaware issued a judgment in VFMCRP’s favor regarding U.S. patent no. 9,561,251

Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Kapruvia® approved in Switzerland with additional regulatory decisions expected in H2 2022: https://mms.businesswire.com/media/20191103005014/en/691947/5/VP_logo_rgb.jpg
Kapruvia® approved in Switzerland with additional regulatory decisions expected in H2 2022


Vifor Fresenius Medical Care Renal Pharma (VFMCRP) and Cara Therapeutics, Inc. (Nasdaq: CARA) today announced that they have received approval for Kapruvia® from the Swiss Agency for Therapeutic

Sonova to accelerate expansion of direct consumer access in Chinese market with acquisition of leading network of clinics
Sonova to accelerate expansion of direct consumer access in Chinese market with acquisition of leading network of clinics
Sonova to accelerate expansion of direct consumer access in Chinese market with acquisition of leading network of clinics
QIAGEN veröffentlicht Nachhaltigkeitsbericht 2021
QIAGEN veröffentlicht Nachhaltigkeitsbericht 2021


QIAGEN (NYSE: QGEN; Frankfurt Prime Standard: QIA) hat große Fortschritte im ESG-Bereich erzielt (Umwelt, Soziales, Governance), die das Unternehmen im heute veröffentlichten Nachhaltigkeitsbericht

QIAGEN Issues 2021 Sustainability Report
QIAGEN Issues 2021 Sustainability Report


QIAGEN (NYSE: QGEN; Frankfurt Prime Standard: QIA) today released its 2021 Sustainability Report, outlining significant achievements in the areas of Environment, Social and Governance (ESG) as part

Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Tavneos® (avacopan) recommended by England’s NICE for the treatment of AAV (GPA/MPA): https://mms.businesswire.com/media/20191103005014/en/691947/5/VP_logo_rgb.jpg
Tavneos® (avacopan) recommended by England’s NICE for the treatment of AAV (GPA/MPA)


Vifor Fresenius Medical Care Renal Pharma (VFMCRP) is pleased to announce that England’s National Institute for Health and Care Excellence (NICE) has recommended Tavneos® in combination with a

Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Premier, Inc. Reports Fiscal-Year 2022 Fourth-Quarter and Full-Year Results: https://mms.businesswire.com/media/20191105005372/en/754182/5/PR_LogoSpec_%282%29.jpg
Premier, Inc. Reports Fiscal-Year 2022 Fourth-Quarter and Full-Year Results


Premier, Inc. (NASDAQ: PINC), a leading technology-driven healthcare improvement company, today reported financial results for the fiscal-year 2022 fourth quarter and full year ended June 30, 2022

Convatec Group PLC: Director/PDMR Shareholding
Convatec Group PLC: Director/PDMR Shareholding
Convatec Group PLC: Director/PDMR Shareholding
Sonova revises FY 2022/23 outlook due to subdued market 
and ongoing input cost challenge
Sonova revises FY 2022/23 outlook due to subdued market  and ongoing input cost challenge
Sonova revises FY 2022/23 outlook due to subdued market  and ongoing input cost challenge
Kampf gegen internationale Gesundheitskrise: QIAGEN bringt syndromischen Affenpocken-Test für QIAstat-Dx-System auf den Markt
Kampf gegen internationale Gesundheitskrise: QIAGEN bringt syndromischen Affenpocken-Test für QIAstat-Dx-System auf den Markt


QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) gab heute die Einführung des QIAstat-Dx Viral Vesicular Panel RUO bekannt – der erste syndromische Test, der zwischen Affenpocken-Erregern

QIAGEN Launches Syndromic Test for QIAstat-Dx Device to Combat Global Monkeypox Health Emergency
QIAGEN Launches Syndromic Test for QIAstat-Dx Device to Combat Global Monkeypox Health Emergency


QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) today announced the launch of the QIAstat-Dx Viral Vesicular Panel RUO, the first syndromic test to differentiate between monkeypox and five

Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc
Form 8.3 - The Vanguard Group, Inc.: Mediclinic International plc