- State-of-the-art Analytical Services facility in the USA
- Physical and Chemical Characterisation
- Method Development and Validation
- API & Drug Product Testing
- Stability Testing
- Impurity Identification and Structure Elucidation Services
- Bioanalytical Services
Method Development and Validation
We provide method development, optimisation and validation services for both API and drug products, to deliver analytical support in:
Our dedicated team of analytical scientists offer a unique blend of experience, expertise and focus to deliver reliable, information-rich methods to meet your exact requirements.
Working closely with clients, we deliver robust and efficient stability-indicating methods. Use of automated method development software, statistical design of experiments and emerging chromatography technology – such as UPLC™ – reduces method development times, providing smart separation solutions for the 21st century.
Validations are conducted under cGMP in compliance with ICH guidelines. The use of Empower 2 Method Validation Software allows us to streamline the method validation strategy. This brings the benefits of minimised time and cost for the validation process, whilst generating accurate and reliable data.
State of the Art Analytical Laboratories
With a recent investment of £9million in state-of-the-art analytical / microbiological laboratories we provide a comprehensive range of analytical solutions.
Over 150 highly qualified, experienced analytical scientists
Integration of Analytical Scientists
We have a wide range of analytical scientists on a single site including; organic chemists, analytical development scientists and commercial quality control analysts.