Once a salt screen or polymorphism project has been completed, customers often want to have access to the additional pharmaceutical development knowledge and techniques available within Charles River to help support their API as it progresses.
With rapid turnaround times, high-quality reports and communication between your team and the Charles River scientists, you can be assured that the data are accurate and produced and interpreted in a timely manner.
- Inhaled formulation – lactose stability/blending
- Excipient compatibility studies – with a range of excipients
- Capsule dissolution studies (non-ICH)