Formulation Analysis

A long, well-organized laboratory bench equipped with advanced analytical instruments, including mass spectrometers connected to computers with monitors displaying operational interfaces. The focus is on the foreground equipment, with a softly blurred background that emphasizes the sophisticated and high-tech environment. This setting represents the cutting-edge tools and technologies used by Alderley Analytical for precise and thorough formulation analysis, ensuring high-quality outcomes in pharmaceutical development.
A laboratory professional at Alderley Analytical carefully loads samples into an advanced analytical instrument, showcasing the meticulous sample preparation process. This step is critical in ensuring the precision and accuracy of the laboratory's bioanalytical testing services, demonstrating their commitment to delivering high-quality results.

We provide an extensive analytical service to ensure accurate formulation and dosing concentrations for successful toxicology studies. Formulation analysis is an essential support service for GLP toxicology studies and is often advisable on non-GLP studies when accuracy of dosing concentration is critical. We offer a comprehensive formulation analysis service by our specialist team. Alderley Analytical has considerable experience in analytical method development and validation, as well as the subsequent analysis of dose formulation samples.

In the high-tech environment of Alderley Analytical's laboratory, a scientist engages with sophisticated laboratory equipment to manage and analyze critical data. This image captures the essence of modern bioanalytical research, showcasing the intersection of science and technology in the pursuit of breakthrough discoveries.

Achieved concentrations of dose formulations is a regulatory requirement for GLP toxicology studies. Analysis of dose formulations, whether solutions or suspensions is required to verify the concentration accuracy and homogeneity of the formulation used for dosing (or in vitro testing) during preclinical programs. Stability of the dose formulations under the conditions of the study is also verified.

Analyses are performed by highly trained personnel who have a wide range of scientific skills and many years of experience. Method development is conducted by experienced staff who are responsible for the efficient transfer of clients’ methods, the development of assays from first principles, or the modification of existing methods as necessary.

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