our services
PRN leverages long-standing relationships with industry experts to provide a comprehensive approach to meet your clinical trial needs.
All Stages of Clinical Trial Management
Project Startup
PRN supports you from study conception and planning to protocol development and site selection. With over 1000 sites across all 50 US states, PRN ensures the best sites at the time of selection.
Clinical Monitoring
Our project managers and clinical research associates average at least 10 years’ experience in clinical monitoring with deep knowledge of ophthalmology. They are thorough, detail-oriented, and exhibit superior professional maturity to represent you well.
Site Auditing
Our experienced team supports a range of QA activities to meet your needs.
Project Completion
PRN study teams are committed to seeing your study through to its completion. This continuity ensures excellence in study involvement and execution.
Regulatory
PRN understands the complexities of navigating through the requirements of regulatory authorities. We partner with the best regulatory affairs specialists to assist you through this complicated process.
Pharmacovigilance
Our pharmacovigilance experts play a crucial role in clinical trials as they monitor safety and efficacy signals and adverse events, and support safety-related regulatory submissions.
Medical Monitoring
Hand in hand with our pharmacovigilance experts, our approachable, board certified ophthalmologists provide medical oversight for your trial, with friendly and timely support to investigators and their research personnel, and your entire clinical team.
Medical Writing
From protocol development to CSR finalization, our medical writers’ detail-oriented, thoughtful and systematic approach provides support where you most need it.
Collaborative Partnership with Our Subject Matter Experts
