The FDA approves oral pritelivir for drug-resistant herpes sores in immunocompromised patients; what it means for antiviral ...

PharmTech covered one of the industry’s biggest events this week, as CPHI Milan was in full force with experts arguing that ...

Medication nonadherence remains one of the widest gaps between how a drug performs in clinical trials and how it performs in ...

The winners of the CPHI Pharma Awards 2026 include a neurodegeneration platform, a track-and-trace packaging innovation, a ...

As publishers and research platforms such as Reaxys and Springer Nature build application programming interface (API) access ...

Access Part 1 of this interview in which Scarboro explains why real-world usability belongs at product definition. Access ...

Mitigating nitrosamine risk requires assessing each product individually, says Bram Baert, Global Head of Regulatory Affairs ...

Shadow AI and vendor data retention put GMP records and trade secrets at risk. AI Pulse Check panelists outline what pharma ...

Equivalence test using two one-sided tests are widely used for demonstrating the comparability of treatment effects in different research fields. The method described in the manuscript aims to use ...

Richard Jaenisch examines whether FDA's NAM pathway truly shortens drug pipelines or just shifts the evidentiary burden elsewhere. Richard Jaenisch and Chris Cole dig into whether New Approach ...

"What matters is that someone owns the entire pathway for that product from identifying the unmet need through development, ...

Jason Bertola, executive director of Commercial Development for the Advanced Synthesis Platform at Lonza in North America, ...