Uniform dose formulation is key to meeting safety study requirements. Homogeneity or uniformity of a dose formulation is a requirement for ensuring integrity of regulated preclinical safety studies.
A Technical Forum featuring representatives from Dow Chemical, ISP, and DMV-Fonterra Excipients. This article is part of PharmTech's supplement "Solid Dosage and Excipients 2010." This article is part ...
Nonclinical dose formulation analysis methods are used to confirm test article concentration and homogeneity in formulations and determine formulation stability in support of regulated nonclinical ...
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