The pharmaceutical industry is witnessing a significant shift in the reformulation of injectable drug products for nasal delivery. This article presents a case study of using modelling to accelerate the reformulation process. The focus is on Nanopharm’s SmartTrack™, a process that combines breath profiles recording with realistic aerodynamic particle size distribution performance testing, in-vitro dissolution, and morphology directed particle sizing and chemical imaging of a representative lung dose and regional deposition modelling.

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Rethinking bioequivalence for nasal suspensions: Adopting an in-vitropathway with confidence
Discover how MDRS provides a regulatory-accepted alternative to clinical endpoint studies for nasal suspension bioequivalence. Learn to de-risk your ANDA pathway today.