Phase I/IIa

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
• Biological/Biosimilar
• Drug Interaction studies
• Modified release formulations
• Transdermal drug delivery
• Inhaled drugs
• PD profiling of pharmacological effects (biomarkers)