Formulation Development White Papers & Articles
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AI Enabled Pharmaceutical Cocrystal Screening
9/3/2026
Cocrystal candidate screening is resource-intensive and prone to gaps. This paper examines how AI-based modeling, trained on more than 20,000 data points, can sharpen candidate prioritization without sacrificing scientific rigor.
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Looking Beyond Solubility And Process Performance
9/2/2026
Solvent selection for spray-dried dispersions significantly impacts drug performance, scalability, and supply chains. Early, structured solvent choice is vital for successful manufacturing and commercialization.
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How To Achieve Late-Phase Success In Complex OSD Development
8/31/2026
Late-phase OSD scale-up demands more than technical know-how. This paper examines the frameworks, tools, and partnership models that determine whether promising molecules reach commercial production reliably.
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Reducing Uncertainty In Early Oral Drug Development
8/31/2026
Five recurring decision points in early oral solid dose development carry outsized downstream consequences. AI/ML-driven predictive modeling is reframing how teams manage those decisions under API and timeline constraints.
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Lipid Formulation Development: Why Softgels Are The Technology Of Choice
8/31/2026
Low bioavailability affects roughly 80% of APIs, yet many drug developers default to standard OSD forms. This paper examines why softgels deserve earlier consideration in formulation strategy.
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5 Hidden Risks In Early-Phase OSD Formulation Development
8/31/2026
Early formulation decisions in OSD development carry risks that may not surface until later stages, when the cost of course correction is significantly higher.
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Overview Of Hot Melt Extrusion And Its Pharmaceutical Applications
8/31/2026
More than 40% of NCEs face aqueous solubility challenges. Here, we examine how hot melt extrusion addresses solubility, modified release, abuse deterrence, and scale-up across pharmaceutical development.
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Enabling Flexibility And Scientific Innovation In OSD Development
8/31/2026
How one clinical-stage CNS biotech navigated early formulation complexity, shifting pipeline priorities, and scalable manufacturing demands through a strategic CDMO partnership.
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Robust Database Characterizes And Optimizes Product Development
8/29/2026
Integrating material characterization data with process parameters accelerates drug development, reduces empirical testing, and strengthens regulatory compliance.
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Optimize Process Performance And Maximize HCP Removal
8/27/2026
Compare filtration strategies and explore how filter selection affects host cell protein removal, processing efficiency, and the balance between impurity clearance and filtration performance.