Clinical Trial Services

Rapid Study Start Up
Quality Clinical Research, Inc has processes in place to efficiently turn around initial documents in > 1 week. Site staff prepares the regulatory packet for time-sensitive start-up activities.  Contracts and budgets are negotiated in house which allows for faster turnaround.


Speedy Recruitment and Retention

Our full-time Recruiting Specialist develops recruiting and screening strategies while waiting for IRB approval. As soon as IRB and Sponsor approval is granted, promotional activities are initiated and screening subject are schedule for initial visits. Our study volunteer database is populated with thousand of volunteers. Our full-time Recruiting 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. We pride ourselves on our history of exceeding enrollment  goals. 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.

Source Prepartion

FDA auditable source documents are prepared on site.  QCR creates separate source documents for each visit that are user friendly. All procedures and information to be collected is in chronological order of collection per protocol requirements. Our Data entry specialist trained on most EDC systems enters source documents within 48 hours of the subject’s visit.  QCR can create source for your next clinical trial.  Please contact Tricia Harrison at tricia@qcromaha.com.