In the latest installment of the PharmTech AI Pulse Check video series, Associate Editorial Director Christopher Cole is ...

This article examines how modern automation platforms create the digital foundation required for Pharma 4.0 by integrating ...

The FDA's expanding embrace of new approach methodologies (NAMs) is forcing pharmaceutical manufacturing and quality teams to rethink how preclinical and CMC data will be generated, validated, and ...

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 ...

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

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

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

Manufacturers are encouraged to treat resiliency policy as an actionable trend and proactively shape solutions rather than ...

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 ...

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

In US regulatory news, the FDA opened applications for its Expedited IND Pilot on September 15. 1 The program pairs drug ...