- Non-GMP Pharmaceutical Development
- Early Stage Development
- Scale Up and Late Stage Development
- Clinical Trial Manufacture
- Contained Development & Manufacture
- Analytical Services
Our radiolabelling facility, which is on the same site as our pharmaceutical development facilities, is licensed by the MHRA to produce GMP radiolabelled materials which can be dosed in humans. This enables us to provide our clients with their radiolabelled drug in a convenient dosage form for the clinic. Typically we prepare capsules or bottles which contain the required dose.
One of the benefits we offer is scientific continuity on every project for every client. If we have already worked with the API, we will have gained valuable experience in working with it in both a manufacturing and analytical testing environment.