Working in partnership to prepare for manufacture
Cambridge Pharma’s expertise in cGMP manufacturing means we are ideally placed to support process development for our clients’ novel drug products.
From our dedicated pilot laboratory, we can provide the complete range of services to develop processes for transfer to sterile manufacturing in our GMP facility ensuring they will be capable for future scale-up when required.
Our experienced team can undertake small-scale batch filling for stability testing and mixing studies, covering both conventional formulations and viscous solutions, gels and suspensions, using a variety of container types and methods. We have particular expertise in container closure integrity testing.
We will work closely with your team to devise and carry out the necessary process development work, delivering clear reports and quality documentation.
Our team of pharmaceutical scientists can provide a range of services including:
- Early stage mixing studies
- Stability batch filling
- Process optimisation and characterisation
- Container closure integrity development and testing
- Onsite GMP standard testing laboratory
- Technical transfer