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European Critical Medicines Alliance - guide — EUbusiness.com | EU news, business and politics

The European Commission's Health Emergency Preparedness and Response Authority (HERA), working with the Belgian EU Presidency, launched on 24 April the Critical Medicines Alliance. The Alliance brings together national authorities, industry, healthcare organisations, civil society representatives, the Commission and EU agencies to identify the best measures to address and avoid shortages of critical medicines.

Belgium , Hungary , Spain , Belgian , European-medicines-agency , Union-list-of-critical-medicines , Commission-health-emergency-preparedness , Response-authority , Battery-alliance , Medicines-shortages-steering-group , European-critical-medicines-alliance

JERAYGO (aprocitentan) recommended for approval in Europe for the treatment of resistant hypertension

Ad hoc announcement pursuant to Art. 53 LR Idorsia receives a positive opinion from the Committee for Medicinal Products for Human Use for JERAYGO™ as the first and only endothelin receptor...

Liechtenstein , Switzerland , Norway , Allschwil , Switzerland-general- , Iceland , United-states , Australia , Swiss , America , Americans , Jean-paul-clozel

Idorsia Pharmaceuticals Ltd: JERAYGO (aprocitentan) recommended for approval in Europe for the treatment of resistant hypertension

Idorsia Pharmaceuticals Ltd: JERAYGO (aprocitentan) recommended for approval in Europe for the treatment of resistant hypertension
finanznachrichten.de - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from finanznachrichten.de Daily Mail and Mail on Sunday newspapers.

United-states , Allschwil , Switzerland-general- , Switzerland , Iceland , Australia , Liechtenstein , Norway , Americans , Swiss , America , Dennis-riedl

JERAYGO (Aprocitentan) Recommended For Approval In Europe For The Treatment Of Resistant Hypertension

(MENAFN - GlobeNewsWire - Nasdaq) Ad hoc announcement pursuant to Art. 53 LR Idorsia receives a positive opinion from the Committee for Medicinal Products for Human Use for JERAYGOTM ... ...

Committee-for-medicinal-products-human , Medicinal-products , Human-use , Com-finance-health-marketing-menafn-pharmaceuticals ,

CHMP Adopts Positive Opinion Recommending Approval of Bristol Myers Squibb's Opdivo® (nivolumab) in Combination with Cisplatin and Gemcitabine for the First-Line Treatment of Adult Patients with Unresectable or Metastatic Urothelial Carcinoma

Recommendation based on results from CheckMate -901, the first Phase 3 trial with an immunotherapy-chemotherapy combination to demonstrate a survival benefit versus standard-of-care chemotherapy...

United-states , Japan , Taiwan , South-korea , China , Bristol-myers-squibb , Dana-walker , European-medicines-agency , Company-opdivo , Twitter , Instagram , Global-program

Apellis Announces Pegcetacoplan MAA Review Has Been Reset to Day 180 of Initial Assessment by European Medicines Agency (EMA)

Apellis Announces Pegcetacoplan MAA Review Has Been Reset to Day 180 of Initial Assessment by European Medicines Agency (EMA)
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Meredith-kaya , Lissa-pavluk , Committee-for-medicinal-products-human-use , Twitter , Apellis-pharmaceuticals-inc , European-medicines-agency , Linkedin , European-union , Exchange-commission-on , Exchange-commission , Nasdaq , Medicinal-products

Apellis Announces Pegcetacoplan MAA Review Has Been Reset to Day 180 of Initial Assessment by European Medicines Agency (EMA)

Apellis Announces Pegcetacoplan MAA Review Has Been Reset to Day 180 of Initial Assessment by European Medicines Agency (EMA)
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Meredith-kaya , Lissa-pavluk , European-union , Nasdaq , Exchange-commission , Exchange-commission-on , European-medicines-agency , Apellis-pharmaceuticals-inc , Committee-for-medicinal-products-human-use , Medicinal-products , Human-use , Private-securities-litigation-reform-act

Apellis Announces Pegcetacoplan MAA Review Has Been Reset to Day 180 of Initial Assessment by European Medicines Agency (EMA)

Apellis Announces Pegcetacoplan MAA Review Has Been Reset to Day 180 of Initial Assessment by European Medicines Agency (EMA)
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Lissa-pavluk , Meredith-kaya , Exchange-commission , Apellis-pharmaceuticals-inc , Nasdaq , Committee-for-medicinal-products-human-use , European-medicines-agency , Exchange-commission-on , European-union , Has-been-reset , Initial-assessment , Medicinal-products

Johnson & Johnson receives positive CHMP opinion for

Johnson & Johnson receives positive CHMP opinion for
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Singapore , Belgium , Saclay , France-general- , France , Beerse , Region-flamande , United-states , American , Nicolas-girard , Henar-hevia , Institut-curie

Bristol Myers Gets CHMP Backing for Opdivo Combo in Bladder Cancer

Bristol Myers Gets CHMP Backing for Opdivo Combo in Bladder Cancer
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Colin-kellaher , Bristol-myers-squibb , Bristol-myers , Drug-administration , European-commission , Myers-squibb , European-medicines-agency , Medicinal-products , Human-use , Dow-jones ,