Feasibility & Patient Access Planning

A thorough feasibility and site selection is the basis of any successful clinical trial. At SIRO, the feasibility process is at the core of our project planning and proposal activity. The feasibility group at SIRO has worked on virtually every therapeutic area and has direct contacts with key investigators and trial sites. With over a decade of experience and collated databases, the feasibility group is to assist and advise clients in their clinical trial plans.

• Experience in most therapeutic areas
• Over a decade and a half of experience and collated databases
• Efficient feasibility assessment process
• Custom-designed feasibility questionnaires
• Constant communication with client

Our study feasibility assessment process is efficient and is capable of identifying the best investigative sites to conduct a clinical trial. Our custom designed feasibility questionnaires and tested processes are effective in predicting site success in implementing a given clinical trial. We are able to predict the recruitment rates with a high degree of accuracy.

The feasibility group works with clients to identify qualified principal investigators quickly from its site database, our experience, site reputation, and where appropriate, a site feasibility visit. Recommendations are based on criteria including:

• Investigator interest
• Number of eligible patients expected to recruit
• Concurrent trial workload, particularly at recruitment stage
• Previous experience in similar clinical studies
• Recruitment & retention in prior clinical trials
• Site personnel study experience and training
• Trial-required facilities such as laboratories and pharmacies
• Trial-specific equipment e.g. measuring and imaging
• Additional sponsor requirements