“The European Medicines Agency might supplant the FDA as the gold standard if the FDA goes off track and is politically ...

J&J’s filing is based on results from the phase 3 AQUILA trial. Among 390 patients with high-risk smoldering multiple myeloma ...

His confirmation has been postponed as he failed to impress MEPs, slipping on reproductive and sexual rights. View on ...

About AVT23 AVT23 is a monoclonal antibody and proposed biosimilar to Xolair ® (omalizumab). AVT23 is an investigational compound and has not received regulatory approval in any country. Biosimilarity ...

The FDA is warning that patients taking GLP-1s may be at a higher risk of inhaling fluid into their lungs while under ...

Modern pharmaceuticals have revolutionised disease prevention and treatment. But eventually, the chemicals can end up in rivers, oceans and soils.

In 2023/24, the EU launched the Critical Medicines Alliance, while the European Medicines Agency has launched a “solidarity ...

Patient involvement in health policy is a patchwork across the EU. Putting the lived experience front and centre of policy-making was prioritised at a recent high-level policy event organised by the ...

The MEPs also criticized Varhelyi over Hungary’s use of the Russian-made Sputnik vaccine during the COVID-19 pandemic, alongside vaccines approved by the European Medicines Agency. He responded by ...