Articles by Amy Smith - Pharmaceutical Technology

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Articles by Amy Smith

Amy Smith


Articles
Determining Potency of Preclinical Dose Formulations
October 2, 2012

Potency is a required measurement to determine the amount of active ingredient contained in a preclinical dose formulation. Assessing potency ensures that the test system receives the appropriate amount of active ingredient based on predetermined specifications.

How to Assess Preclinical Dose Formulation Homogeneity
July 2, 2012

Uniform dose formulation is key to meeting safety study requirements.

Preclinical Dose-Formulation Stability
June 2, 2012

When designing stability protocols, formulation, storage, and dosing conditions must be assessed.

Preclinical Dose-Formulation Stability
June 1, 2012

A number of factors need to be considered when evaluating preclinical dose-formulation stability. The authors discuss formulation, storage and dosing conditions.

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Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
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