Formulation development
With a team of seasoned experts and over a thousand projects resolving some of the most complex drug and formulation issues we bring our innovative research approach to formulation development. Whether it is fast development (less than 24 weeks) for first time in human trials or complex controlled delivery we find a formulation solution that fits the properties of the molecule and the intended use. We work with most materials including poorly water soluble, potent and cytotoxic compounds.
Our approach is based around understanding three key parameters; the physicochemical properties of the drug, the disease and the destination of delivery. Our services for formulation development for capsules, tablets and liquids includes:
- Prototype development and testing
- API characterisation (preformulation)
- Enhanced dissolution screening
- Excipient compatibility screening
- Process development, validation and scale-up batches
- Cleaning method development and validation
- Analytical development and validation (assay / related substances)
- Stability (informal and ICH)
- Methods transfer and management of cGMP manufacturing
Our scientific panel of experts can provide you strategic consultancy for the development of your pharmaceutical products. Read more