Working with the Monitor's Favorite

Rapid Study Start Up

Solano Clinical Research has processes in place to efficiently turn around initial documents such as the CDA, CTA and budget. Study Coordinators prepare the regulatory packet for submission to a central IRB to get approval within 2 to 3 weeks. Simultaneously, team members prepare for time-sensitive start-up activities.

Speedy Recruitment

Our full-time Recruiter/Retention Specialist develops recruiting and screening strategies while waiting for IRB approval. As soon as IRB approval is granted, promotional activities are initiated and initial screening starts. Our study volunteer database is populated with hundreds of healthy volunteers and those with indications.

High Enrollment and Retention

Our full-time Recruiter/Retention Specialist pays careful attention to selection criteria to ensure a higher probability of study completion. Regular follow up calls are made to ensure compliance with study requirements and keeping appointments. In the last 2 years, we have exceeded enrollment in 12 studies. Our retention rate is 90%+.

Clean Data

We are able to deliver clean data to clients because of GCP, ICH and FDA 21CFR compliance and well established standard operating procedures to ensure study success, low query rates and favorable audits. We frequently have the lowest number of queries per study among multiple sites.