The protocol is a core part of any clinical research project.

Our network of contacts with expert clinicians enables us to provide state-of-the-art medical and scientific input to your protocol design.

However, studies must also be practical and realistic – our team of experienced researchers will ensure that the study objectives can be achieved in a timely and effective manner. This means that sites will be motivated to recruit patients to the study and patients will be keen to take part.

Our experience has demonstrated that pharmacist input in protocol design is essential to ensure smooth study feasibility and significantly reduce study set-up time. Our pharmacy advisors have extensive experience in reviewing research protocols both at national and a global level.