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38 recent stories.

European Parliament hemicycle Brussels 200406.jpg

Policy / European Union

PRIME Scheme: Fast-Tracking Revolutionary Medicines in the EU

The European Medicines Agency's PRIME initiative aims to expedite the development and assessment of innovative treatments, focusing on medications addressing high unmet medical needs.

Explained Affected: Businesses, Workers European Union

08 May 2026

European Parliament hemicycle Brussels 200406.jpg

Policy / European Union

EU Agency Approves Dengue Vaccine for Use Outside Europe

The European Medicines Agency has issued a positive opinion on the Dengue Tetravalent Vaccine (Live, Attenuated) created by Takeda for use outside the EU, highlighting its effectiveness in preventing severe dengue disease in children and adolescents.

Updated Affected: Workers, Local governments European Union

08 May 2026

First European Parliament Hemicycle, Robert Schuman building, 1973.jpg

Policy / European Union

EU Evaluates Safety of Combined Pain Relief Medicines

The European Medicines Agency has initiated a safety review of certain combination pain relief medications, including those containing buclizine and codeine. The decision reflects ongoing efforts to ensure the safety of pharmaceutical products in the EU.

Updated Affected: European readers European Union

08 May 2026

European Parliament hemicycle Brussels 200406.jpg

Policy / European Union

EMA Approves Strimvelis: A Groundbreaking Gene Therapy for ADA-SCID

Strimvelis, an innovative gene therapy for treating severe combined immunodeficiency due to adenosine deaminase deficiency (ADA-SCID), has been approved for use in the EU, offering hope to patients without suitable bone marrow donors.

Updated Affected: European readers European Union

08 May 2026

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 4-7 May 2026

Policy / European Union

European Medicines Agency's PRAC Meeting: Key Updates from May 2026

The Pharmacovigilance Risk Assessment Committee (PRAC) of the European Medicines Agency reviewed crucial safety policies during its May meeting, highlighting no new safety referrals or urgent actions.

Updated Affected: European readers European Union

08 May 2026

First European Parliament Hemicycle, Robert Schuman building, 1973.jpg

Policy / European Union

Pregabalin Viatris: New Insights into Its Authorisation and Use

Pregabalin Viatris, a generic form of the widely used medication Lyrica, has been formally recognised by the European Medicines Agency for its efficacy in treating neuropathic pain and anxiety disorders in adults.

Updated Affected: Businesses, Workers European Union

08 May 2026

EASA issues SIB on safe usage of Jet A aviation fuel in Europe

Society / European Union

EASA Advises on Safe Use of Jet A Fuel Amidst Supply Shortages

The European Union Aviation Safety Agency (EASA) has issued a Safety Information Bulletin (SIB) concerning the potential use of Jet A fuel in Europe due to disruptions in the supply of Jet A-1 grade fuel.

Updated Affected: Travelers, Businesses European Union

08 May 2026

Pre-flight pints: Should alcohol be served at the airport before morning flights?

Society / Europe

Pre-flight Pints: The Debate on Airport Alcohol Sales

As airports serve alcohol throughout the day, a debate ignites over early morning drinking. Ryanair's CEO calls for restrictions, citing unruly behavior on flights.

Updated Affected: Travelers, Businesses Europe

08 May 2026

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Policy / European Union

Dupixent: A Breakthrough Treatment for Chronic Inflammatory Conditions

Dupixent (dupilumab) has been officially recognized for its efficacy in treating various chronic inflammatory diseases, marking a significant advance in therapeutic options since its authorization in 2017.

Updated Affected: European readers European Union

08 May 2026

European Parliament hemicycle Brussels 200406.jpg

Policy / European Union

EU Approves Mysildecard for Treating Pulmonary Arterial Hypertension

Mysildecard, a generic form of sildenafil, has received EU approval for treating pulmonary arterial hypertension in both adults and children. The treatment aims to improve exercise capacity by dilating blood vessels in the lungs.

Updated Affected: Businesses, Local governments European Union

07 May 2026

Society / European Union

Febuxostat Viatris: EU Approval for Gout Treatment and Hyperuricaemia

The European Commission has granted indefinite marketing authorization for Febuxostat Viatris, a generic medication indicated for treating high uric acid levels in gout sufferers and cancer patients undergoing chemotherapy. Approved since June 2017, the drug is recognized for its efficacy and safety profile, presenting a viable option within the region.

Updated Affected: Businesses, Local governments European Union

07 May 2026

Policy / European Union

EU Approves Darunavir Viatris for HIV Treatment

The European Medicines Agency has authorized Darunavir Viatris, a generic antiviral medication for treating HIV-1 infection, emphasizing its bioequivalence to the reference drug Prezista.

Updated Affected: Businesses, Workers European Union

07 May 2026

Society / European Union

European Commission Withdraws Marketing Authorization for Rapilysin

The European Commission has officially withdrawn the marketing authorization for Rapilysin, a treatment indicated for myocardial infarction. The decision was initiated by the product's holder, Actavis Group, due to commercial reasons.

Updated Affected: Businesses, Workers European Union

07 May 2026

Policy / European Union

European Medicines Agency Authorizes Loqtorzi for Cancer Treatment

Loqtorzi, a monoclonal antibody for cancer treatment, receives EU marketing authorization due to its promising efficacy in extending survival for patients with advanced nasopharyngeal and esophageal cancers, despite known side effects.

Updated Affected: Businesses, Workers European Union

07 May 2026

Society / European Union

European Parliament Considers Security and Defence in Transport

A recent committee meeting at the European Parliament focused on the intersection of security and transport policies. Stakeholders are urged to address these critical issues amid rising global tensions.

Updated Affected: Travelers, Businesses European Union

07 May 2026

Society / European Union

Atazanavir Viatris: New HIV Treatment Approved in Europe

The European Medicines Agency has granted marketing authorisation for Atazanavir Viatris, a new generic HIV treatment that promises to be an effective option for patients aged 6 and over, particularly alongside low-dose ritonavir.

Updated Affected: Businesses, Farmers European Union

07 May 2026

Society / European Union

EU Recommendations for 2026/2027 Seasonal Flu Vaccine Composition

The European Medicines Agency has outlined new strain recommendations for the upcoming flu season, eliminating the need for the B/Yamagata strain as it is no longer circulating.

Updated Affected: Businesses, Local governments European Union

07 May 2026

Policy / European Union

European Medicines Agency Authorizes Uplizna for Rare Autoimmune Conditions

Uplizna (inebilizumab), effective for reducing NMOSD and IgG4-related disease symptoms, has gained conditional approval in the EU. Key usage protocols and safety guidelines are outlined for healthcare providers.

Updated Affected: European readers European Union

07 May 2026

Society / European Union

Olumiant (baricitinib) Authorized for Multiple Conditions in Europe

The European Medicines Agency has confirmed the ongoing authorization of Olumiant, a drug prescribed for moderate to severe rheumatoid arthritis, atopic dermatitis, alopecia areata, and juvenile idiopathic arthritis. Originally approved in 2017, this drug has shown significant efficacy and safety in clinical trials.

Updated Affected: European readers European Union

07 May 2026

Society / Europe

Meta Asks Judge to Overturn Verdict in Landmark Social Media Addiction Trial

Meta has requested a judge to reverse a recent jury verdict that found the company negligent in the design of its platform, which allegedly contributed to a user's depression and addiction. The outcome of this case could have significant implications for social media litigation in the U.S.

Updated Affected: Businesses Europe

07 May 2026

Policy / European Union

EMA Endorses Kerendia for Kidney and Heart Disease Treatment in Diabetes Patients

The European Medicines Agency has authorized Kerendia (finerenone), a new treatment for adults with chronic kidney disease linked to type 2 diabetes, citing its benefits in slowing kidney function decline and reducing cardiovascular risks.

Updated Affected: Businesses European Union

07 May 2026

Policy / European Union

Oncaspar Approved for Cancer Treatment in Europe

Oncaspar, a cancer drug for treating acute lymphoblastic leukaemia in both adults and children, has been authorized by the European Medicines Agency, offering new hope for patients including those allergic to previous treatments.

Updated Affected: Businesses European Union

07 May 2026

Policy / Europe

Germany's Ruling Coalition Divided Over MP Pay Increases

As Germany's Bundestag prepares for automatic pay rises for MPs, tensions arise between conservatives and the center-left over the appropriateness in the current economic climate.

Updated Affected: Businesses, Workers Germany

07 May 2026

Society / Europe

'Dark patterns': Investigating online manipulation

Ireland's media regulator is investigating Meta for allegedly employing manipulative design tactics on Facebook and Instagram, violating the European Digital Services Act.

Developing Affected: Businesses Ireland

07 May 2026

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Policy / European Union

European Medicines Agency Authorises Usgena, a New Biosimilar Treatment

The European Medicines Agency (EMA) has granted authorisation for Usgena, a new biosimilar medicine based on ustekinumab, used to treat plaque psoriasis, psoriatic arthritis, Crohn’s disease, and ulcerative colitis.

Updated Affected: European readers European Union

07 May 2026

Society / European Union

EMA launches new advisory group on vaccine confidence

The European Medicines Agency has established a new advisory group aimed at tackling vaccine hesitancy and improving public trust in vaccination.

Updated Affected: European readers European Union

07 May 2026

Society / European Union

EU-OSHA Shifts Social Media Focus to Bluesky and LinkedIn

The European Agency for Safety and Health at Work (EU-OSHA) announces its departure from X, redirecting its communication efforts to Bluesky and other platforms to continue promoting workplace safety.

Updated Affected: European readers European Union

07 May 2026

Briefing list

Get rule changes before they reach the airport queue.