We carry out a feasibility study on behalf of our customers which includes:

Contacting the right calibre of investigators to establish their interest in conducting the trial and reviewing the protocol either in draft or final version with them.

Checking patient populations and prevalence of disease in different countries depending on the study and marketing requirements and regulations.

Establishing the most current Regulatory requirements of each country where the trial will be conducted and anticipating timelines.

Establishing communication with third party vendors e.g. Central laboratories and checking timelines, workload and cost savings with them.

Quality Assurance of potential short listed investigative sites or third party vendors.

Establishing ahead of time the clinical team via anticipated level of relevant experience that best suits our customer's needs.