Our Clinical Research Resources for Sponsors & CROs
PRI works closely with and meets the needs of the pharmaceutical industry and clinical research organizations.
Clinical trials at our site are always completed on time and with accuracy; we consistently exceed sponsor expectations for integrity, subject enrollment, human protection and expeditious delivery of accurate evaluable data.
PRI is a unique and innovative resource for Phase I-IV clinical trials. Our site is known for effectively combining strategic volunteer recruitment and retention with high-quality clinical research procedures. Our approach is uncompromising—each study conducted at our site is carefully planned and executed according to regulations with superior quality.
PRI is a virtual trial capable, certified SRCS Member site.
Added Clinical Value:
- Direct connection with healthcare issues through day-to-day contact with volunteers
- Expertise in medical science
- Thought leadership in clinical research
- Thorough understanding of regulatory requirements
Added operational value:
- Rapid enrollment through our global reach and strong subject database
- In-house quality assurance
- Experienced, clinically oriented company management and leadership
- Experienced, research educated study coordinators