Hamilton biochemicals has teamed up with a European vialling company. This gives us the opportunity to offer a complete package to our clients. Not only can we manufacture your product to cGMP but also vial the compound, sterile and pyrogen-free, for your clinical trials from Phase I through to Commercialisation.

Our customers benefit from a vast range of services at the various production stages, and a guarantee of assistance throughout the manufacturing process. We offer lot production for clinical studies in line with Good Clinical and Manufacturing Practices; ongoing stability studies providing the yearly controls prescribed by regulations regarding the stability of products, and ICH stability tests.

If you require your API to be vialled for clinical trials then please contact Hamilton biochemicals by phone or email so that we can discuss your requirements in more detail.