Partner with CRP to connect your patients with innovative treatments and advance medical science together.
Give your patients access to investigational medications and therapies before they reach the market.
Participants receive regular monitoring, lab work, and specialist attention throughout the study at no cost.
CRP handles all study coordination, regulatory compliance, and patient management. You refer, we do the rest.
Your patients receive compensation for their time and travel, plus free transportation to study visits.
CRP has conducted over 500 clinical trials since 1996. Your patients are in experienced, FDA-regulated hands.
Receive updates on your referred patients and a follow-up letter at study completion for their medical records.
Use our provider portal to refer patients directly to enrolling studies. We handle screening, enrollment, and all study-related care.
Grant CRP access to your electronic medical records. We use data analytics to identify eligible patients from your existing population, with patient consent.
Join as a sub-investigator on active studies. Conduct visits at CRP or your own office. We match studies to your specialty and patient base.