We have developed many multi-step routes to make preclinical and early clinical phase APIs and intermediates. Services provided include:
Custom synthesis on laboratory to pilot plant scale (cGMP and non-GMP)
- Route selection and safety evaluation
- Process optimisation, scale-up and validation
- Custom synthesis to support medchem , with rapid scale-up of lead candidates
- Preparation of impurities and reference standards
To support such synthetic and manufacturing programmes we offer services including:
- Salt screening and crystallisation studies
- Stability studies (stress tests, accelerated and long term)
- Analytical method development and validation
- Impurity profiling
We also have expertise to develop technologies for production of intermediates pharma and non-pharma application, fine chemicals, F&F ingredients in multi ton scale.
All our processes are designed to be reproducible, transferable, quality compliant, economical and environmentally acceptable.
