Trial Execution

Armed with a well-designed protocol, Centerphase provides timely and predictable clinical trial execution through three key strategies:

Informed Site Selection

Centerphase’s scorecard for study executability is a valuable tool in assessing the types of sites best suited for a trial and the operational risks that may require mitigation. Centerphase provides valuable insights about specific findings which are generalizable to all sites and likely to impact the sponsor's ability to complete the study in a timely and predictable manner.

Activate Sites Efficiently

Centerphase has created a series of innovative operating procedures and to help expedite study start-up and trial activities. Centerphase has developed unique and proprietary technologies to support the monitoring and controlling of key administrative responsibilities. Our focus is to drive efficient budgeting, contracting, IRB review, and subject enrollment that results in significantly shorten cycle-times.

Setting Sites Up for Success

In addition to supporting efficient site activation, Centerphase works with clinical investigators to develop proactive recruitment and retention action plans by leveraging Mayo Clinic's extensive electronic medical records system to identify pre-qualified candidates. Further, we work to translate the protocol into practice via the development of comprehensive study implementation plans to help accelerate the protocol learning curve and ensure quality as well as timely study implementation.