Scientific excellence to support your product
With a dedicated cGMP laboratory in-house, we have extensive testing experience in incoming material, in-process, stability and release for clinical products.
This analytical capability means that we are able to support our customers through the key stages of testing and validation that are critical to a successful product launch.
Our team will work with you to design appropriate stability protocols or programs for execution, then carry out and document all necessary testing to cGMP standards.
Our team of pharmaceutical scientists can provide a range of services including:
- incoming material testing
- in-process controls
- stability testing
- release testing
- method transfer and validation
- full range of analytical techniques
- QP sign off
We put our manufacturing expertise at your disposal, accelerating development of the fill-finish process