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Tablet Formulation Development

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Understand powder behavior to develop robust formulations. Study formulation blends and manufacturing processes following USP <1062> guidelines with our pharmacists to meet tablet Critical Quality Attributes (CQAs) such as dissolution, disintegration, or tensile strength. As an example, assess the impact of dry granulation process on flowability and re-compactibility with minimal amount of material.

Maximize production output, control cost, and keep quality in mind. Compaction simulators are essential to foresee potential tablet defects and solve them during development stage. For example, sticking can be related to temperature or tooling surface which can be evaluated with our formulators prior scale-up.

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