Within our formulation labs and GMP-compliant facility, we primarily provide development and sterile contract manufacturing services that take place in our class (C) 10,000 cleanroom, created to provide flexibility to meet your clinical trial and commercial supply needs. With specialist expertise in developing and manufacturing novel, difficult and dangerous drugs, we support limited-run formulations, products and devices for -
- Formulation development
- Early medical research and pre-clinical studies
- Phase I, II or III clinical trials
- Commercial launch
- Commercial product supply of licensed products in niche/low volume markets
Our flexible approach means drug products, whether liquids, gels or powders, can be delivered in a range of presentations including -
- Ampoules
- Bottles
- Vials
- Cartridges
- Syringes
We undertake contract manufacturing including device assembly, injectables, ophthalmic eye drops and aerosols, with all of the necessary packaging, documentation and technical support services. We are also able to support non-sterile manufacturing projects that involve creams, capsules and ointments.
Please browse the links above or below to find out more information about our specialist clinical manufacturing, contract filling and sterilisation services. These includes:
- Sterile manufacturing and filling (terminal sterilisation)
- Aseptic filling (using isolator technology)
- Filling of c14 radio-labelled/radiolabeled compounds
- Dedicated potent suites to fill/finish cytotoxics and cytostatic products
- In-house testing including sterility, endotoxin, microbiology and analytical chemistry
- Non-sterile manufacturing
- Clinical packaging
In addition, we can support the following -
- Projects involving small molecules
- Process development and validation
- Quality release and QP consultancy
- Gateway testing and release (for US companies)
- Drug/medical device filling and assembly
For information on any of the above, contact us today.









