The US Food and Drug Administration (FDA) has debuted a framework that is designed to help companies move away from the use of non-human primate preclinical toxicology testing. Image credit: ...

Researchers at the University of Plymouth are leading an innovative initiative to advance the study of meningiomas in NF2-related schwannomatosis (NF2-SWN). Meningiomas, often linked to the loss of ...

The ABPI says that industry and academia must come together to bridge the gap between academic and commercially ready preclinical models.

Dublin, Jan. 19, 2026 (GLOBE NEWSWIRE) -- The "Preclinical Bioanalytical Testing Services Market Size, Share & Trends Analysis Report by Molecule (Small, Large), Test (ADME, PD, PK), Workflow, End Use ...

WEST LAFAYETTE, Ind.--(BUSINESS WIRE)--MED Institute, a leader in pre-clinical and clinical medical product development services, is proud to announce a strategic collaboration with Sus Clinicals, a ...

Approximately 75% of anticancer drugs must be tested against paediatric cancer. Drug developers can now use a database of patient-derived tumour models to screen their products for paediatric cancer ...

To test new stroke treatments, a research team from the Keck School of Medicine of USC develops a more rigorous system for conducting preclinical research that could lead to more successful clinical ...

'OPENING THE DOOR': FDA's Joseph Contrera claims the new testing guidelines will encourage innovation. The Food and Drug Administration (FDA) is considering a plan to revise a 25-year staple of ...

Carlin is a vice president at Pathway Policy Group and a veterinarian. Paragas is the CEO and founder of DVLP Medicines and a virologist. The Food and Drug Administration’s recent decision to phase ...