As a full service Contract Research Organisation, we offer vast experience in the management of early phase clinical trials across a broad range of therapeutic areas.
We have a highly experienced scientific affairs team who is ready to advise and help you with your request.
Our broad expertise includes the following areas:
- First-in-Human (FIH) safety and tolerance studies
- Food effect, gender effect, age effect, patient studies
- Bioequivalence and comparative bioavailability studies
- Drug Interaction studies
- Modified release formulations
- Transdermal drug delivery
- Inhaled drugs
- PD profiling of pharmacological effects (biomarkers)