Pharmaceutical R&D teams must accelerate innovation while managing complex scientific data, disconnected research systems, and increasing regulatory expectations. This white paper explores how integrated lab informatics can create a connected digital foundation for research, linking data, workflows, instruments, and teams across the R&D lifecycle. Discover how modern informatics can strengthen collaboration and reproducibility, automate routine processes, and enable more confident, data-driven decisions in drug discovery and development.
Ron Scarboro, Azurity Pharmaceuticals, explains how cross-functional development, disciplined reformulation, and post-approval metrics can help proven medicines work in everyday use.
The FDA approves oral pritelivir for drug-resistant herpes sores in immunocompromised patients; what it means for antiviral development and manufacturing.
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 simulations in Microsoft Excel to compute power for 2 one-sided tests for two groups with unequal variances.
Susan J. Schniepp, distinguished fellow with Nelson Labs, and Siegfried Schmitt, PhD, vice president, Technical, with Parexel, clear up some of the confusion about what does and does not need to be complied with regarding standards set by international pharmacopoeias.