The American Association of Pharmaceutical Scientists (AAPS) will open its 2026 PharmSci 360 meeting on October 25 with a plenary on making the drug development pipeline more efficient, according to an AAPS press release issued October 22, 2026.1 The speaker, Julie Louise Gerberding, MD, MPH, president and CEO of the Foundation for the National Institutes of Health (FNIH), will give her talk, titled "Adaptive Intelligence: Accelerating Biomedical Innovation." PharmSci 360 will run October 25-28 at the Ernest N. Morial Convention Center in New Orleans, Louisiana.1
Key facts
- Event: AAPS PharmSci 360 2026
- Dates: October 25-28, 2026
- Venue: Ernest N. Morial Convention Center, New Orleans, Louisiana
- Opening plenary: Julie Louise Gerberding, MD, MPH (FNIH), October 25
- Talk title: "Adaptive Intelligence: Accelerating Biomedical Innovation"
- Topics: Novel alternative methods, AI, adaptive trial innovations
- Closing plenary: David Berry, MD, PhD (Averin Capital), October 28
- Workshop: AAPS–USP standards workshop, October 26-28
- AAPS leadership: Patrick J. Sinko, PhD, RPh, named chief science officer
"Everyone wants faster drug development. The real challenge is not simply accelerating individual activities but redesigning the development paradigm itself," said Parag Kolhe, PhD, chair of the AAPS 2026 PharmSci 360 Scientific Programming Committee, in the press release.1 "Dr Gerberding will share a compelling vision for a more cyclical, parallel, and integrated approach that has the potential to compress timelines while preserving scientific rigor and quality."
What will Dr Gerberding's plenary cover?
The talk will focus on integrating emerging approaches to product development, including novel alternative methods, artificial intelligence (AI), and adaptive trial innovations, to improve the efficiency and safety of translational medicine.1 Dr Gerberding previously directed the US Centers for Disease Control and Prevention from 2002 to 2009 and has held executive roles at Merck.2
How does the theme connect to regulatory change?
The plenary's emphasis on alternative methods tracks a shift at FDA. On April 10, 2025, the agency announced a plan to phase out animal testing requirements for monoclonal antibodies and other drugs. The plan encourages new approach methodologies such as AI-based computational models of toxicity and laboratory tests using cell lines and organoids.3 FDA has said it would welcome such data in investigational new drug applications, beginning with monoclonal antibody therapies.3
PharmSci 360’s program reflects similar themes. On October 28, Thomas Hartung, MD, PhD, of the Johns Hopkins Bloomberg School of Public Health, will lead an innovator-curated track on new testing approaches, including AI applications, organ-on-a-chip models, and neural organoids.2