NUVISAN’s formulation analysis services include stability testing of the formulation, complementing our in vitro and in vivo toxicity studies and analytical method validation. Our experts can develop and validate methods in our laboratories to support your in vivo toxicity safety package.
To support your project’s specific needs, our laboratories facilitate the analysis of a range of different formulations. For example, the test item can be analyzed in different matrices (e.g., PEG, CMC, and more), such as solutions, emulsions, and suspensions.
All formulation analysis services can be performed under GLP conditions. Accordingly, from start to finish, our chemists collaborate closely with you and our toxicologists to ensure the highest quality of data and results. Likewise, data reporting conforms with common standards, including according to SEND and the FDA.