“ Our direction is consistent and disciplined: deliver on the AI agenda, reinforce prevention-focused infrastructure and scale our capabilities internationally through structured partnerships. ”
2026 could mark a turning point for biosimilar adoption in the US. By scrapping requirements for redundant clinical trials and pushing Congress to end the “Interchangeable” label, the FDA has cleared the runway for biosimilars. However, with PBM “rebate walls” and patent thickets still standing, will these lower cost therapies finally take off in the…
In 2024, contract manufacturers WuXi Biologics and WuXi AppTec were catapulted into global consciousness as two of five Chinese service providers deemed a US national security threat in a draft for a new BIOSECURE Act. While the final version of the law, signed by President Donald Trump in December 2025, was softer than the…
Lyon – recently announced as the host of BIO-Europe Spring 2027 – has long played a vital role in global health and, in 2026, it stands as one of Europe’s most investable life sciences hubs. While less well-known internationally than Basel, Barcelona, London, or Paris, Lyon stands out from the pack through its tightly knit…
“ Hong Kong's Centre for Medical Products Regulation is planned to conduct its first primary review within this year. This represents rapid movement from concept to implementation ”
“ The burden of rare disease in the region is substantial. We are speaking about a rare patient population of approximately 25 million, comparable to the US and Europe, with a high incidence of metabolic, haematological, and neurological diseases ”