On 1 December, the fortunes of the UK pharma sector changed radically, with the UK Government becoming the first in the world ...

If Richard Padzur retires, he would become one of several high-ranking FDA officials who left the agency in 2025.

Citizen Health has entered a multi-year strategic partnership with UCB for expediting drug development across five rare ...

New non-primate draft guidance follows the FDA's wider aim to curtail the use of animal testing in preclinical toxicology.

Rare disease research faces complex regulations, small patient populations, and high costs. As traditional incentives wane, ...

AGC Biologics is set to expand its Cell Line Development Centre of Excellence through a partnership with ATUM.

The World Health Organization (WHO) predicts that fewer than 10% of eligible patients will have access to GLP-1RAs by 2030.

Patient advocacy and industry bodies welcomed the bill’s backing, though it will now need to be passed in the Senate.

Biotechs in the charter city of Próspera aim to cure ageing, but experts question the feasibility of their goals.

If approved, Regeneron and Tessera's TSRA-196 could become the first curative therapy to reach patients with AATD, who have ...

The UK becomes the latest country in President Donald Trump’s long line of trade agreements, though it is the first region to ...

Data management in oncology clinical trials features multiple complexities, and choosing the right EDC system is essential.