Our study feasibility assessment process is efficient and capable of identifying the best investigative sites to conduct a clinical trial.
We are able to predict recruitment rates with a high degree of accuracy.
Recommendations are based on criteria including:
• Investigator interest
• Number of expected eligible patients to recruit
• Concurrent trial workload, particularly at recruitment stage
• 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
For more information, please contact us.