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Liechtenstein Reaffirms Global Leadership in Stability and Philanthropy
Zevra Therapeutics Submits Marketing Authorization Application to European Medicines Agency to Review Arimoclomol for the Treatment of Niemann-Pick Disease Type C
Leqembi®∇ (lecanemab) is the First Medicine that Slows Progression of Early Alzheimer’s Disease to be Authorized in the European Union
EURneffy® 1 mg (adrenaline nasal spray) Recommended for Approval in the EU for Emergency Treatment of Type 1 Allergic Reactions, including Anaphylaxis in Children Weighing ≥15 kg to <30 kg
4BIO Capital Portfolio Company Araris Biotech to be Acquired by Taiho Pharmaceutical for up to USD 1.14 billion
Fajon na Svetu OZN za človekove pravice: Molk ob kršitvah ni nevtralnost — je sokrivda

Fajon na Svetu OZN za človekove pravice: Molk ob kršitvah ni nevtralnost — je sokrivda

Slovenia and Switzerland: Strong economic partners and good friends

Slovenia and Switzerland: Strong economic partners and good friends

bonyf – A Year of Certification, Innovation and Commercial Acceleration
Alvotech and Teva Secure U.S. Settlement Date for AVT06, a Proposed Biosimilar to Eylea®
CEO Insight Releases New 2026 Issue Examining Trust, Governance and Global Connectivity
Regulating Artificial Intelligence in a Fragmented World — RegulatingAI Podcast
Alvotech and Teva Secure U.S. Settlement Date for AVT06, a Proposed Biosimilar to Eylea®
bonyf AG receives the EU-MDR Certification Class IIa for PerioCream
Strong Cresemba® (isavuconazole) sales performance in Europe triggers USD 30 million milestone payment to Basilea
The European Magazine Releases Its Winter 2026 Edition
Dental Prosthetics Market Size to Grow from USD 9.12 Billion in 2024 to USD 15.88 Billion by 2034, at a 5.7% CAGR
SEALSQ C-Suite Visits India to Advance Post-Quantum Semiconductor Personalization Center, Quantum Investments, and Sovereign Space Capabilities
Autolus Therapeutics’ CAR T Therapy AUCATZYL® (Obecabtagene Autoleucel) Granted European Marketing Authorization for Adult Patients (age 26 and older) with Relapsed or Refractory B-Cell Precursor Acute Lymphoblastic Leukemia (R/R B-ALL)
Krystal Biotech Announces European Commission Approval of VYJUVEK® for the Treatment of Dystrophic Epidermolysis Bullosa
argenx Announces European Commission Approval of VYVGART Subcutaneous Injection for Chronic Inflammatory Demyelinating Polyneuropathy

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