In the second session of Nanopharm’s fireside series in partnership with FLUIDDA, industry experts Drs. Will Ganley and Eleanor Canipa from Nanopharm and Dr. Jan De Backer from Fluidda provide their thoughts on what the updated PSGs and alternative bioequivalence tell us about the FDA’s position on inhaled generics.

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GDUFA: FDA adds further weight to modelling and simulation’s role in bioequivalence
GDUFA 2026: FDA strengthens role of modeling & simulation for inhaled generic drug bioequivalence. Learn how this shift enhances efficiency for OINDP development.
