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Solid-form screening is a foundational step in pharmaceutical development because the physical form of an active pharmaceutical ingredient can influence stability, manufacturability, dissolution, and downstream formulation strategy. Polymorphs, cocrystals, and salts each expand the developable form landscape, but they also increase the complexity of experimental exploration. Current solid-form screening workflows often rely on expert-designed experimental grids, manual interpretation of characte
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Al-Mahdi et al. (2026) studied this question.
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