From discovery through post-approval, analytical development is a critical part of the drug development process occurring throughout all stages with strict guidelines
With analytical capabilities, scientific expertise and state-of-the-art instrumentation to support all stages drug development, Eurofins BioPharma Product Testing can support the development and validation of virtually any test for your starting material, API, finished product, intermediate or packaging under cGMP guidelines.
Having developed thousands of analytical methods using a wide range of technologies, ranging from routine to specialized methods, Eurofins BioPharma Product Testing supports all aspects of analytical development, including:
- Method Development and Validation
- Comparator Product Testing
- Impurities Testing
- Stability Indicating Methods
- Non-Compendial Raw Materials