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.
Boyang Wang, Immortal Dragons, explains how FDA’s Expedited IND Pilot and research partners could speed serial steps to first-in-human trials compared to China’s 818 Decree.
This article examines how modern automation platforms create the digital foundation required for Pharma 4.0 by integrating manufacturing systems, centralized data management, Industrial Internet of Things connectivity, electronic batch production records, and AI-driven analytics.
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.