Developing an IVRT testing method for the validation of semis-solids

The effective measurement of drug release of an active pharmaceutical ingredient (API) from a dosage form plays a critical role in both formulation design and control of finished pharmaceutical products. The evaluation method used is determined by a variety of factors, including the dosage form itself and the intended route of delivery. 

Recipharm’s IVRT method provides an efficient method for the evaluation of drug release from semi-solid topical formulations, with the technique’s use increasing as both a development tool and means of setting product specifications.

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