Reaching a rare patient population on time
The study reached its enrolment target and moved to database lock on schedule.
Contract Research Organisation · Since 2008
Precision proves your success.
WR Clinicals Inc. designs and delivers clinical trials across Eastern Europe, the EAEU and Central Asia — and now brings that expertise to US sponsors. Powered by our own patient recruitment software.
Eastern EuropeEAEUCentral AsiaUSA — new
70+Clinical trials completed
2,000+Patients enrolled across all countries
100+Investigator sites in our network
2008Year founded
- Oncology
- Cardiology
- Ophthalmology
- Nephrology
- Urology
- Infectious Diseases
- Orthopedics
- General Surgery
- Pediatrics
What we do
Full-service clinical research, from protocol to report
Integrated services, one accountable team. Use them together or choose exactly what your study needs.
Phase I–IV Clinical Trials
From first-in-human studies to post-marketing surveillance, we run Phase I–IV trials end to end: feasibility, site selection and start-up, monitoring, data management and close-out.
Learn more →Medical Device Clinical Trials
We support pre-market and post-market clinical investigations of medical devices, including first-in-human, pivotal and post-market clinical follow-up studies.
Learn more →Medical Writing
Clear, scientifically rigorous documents shorten approval timelines.
Learn more →Pharmacovigilance
Patient safety is non-negotiable.
Learn more →Biostatistics & Data Programming
Good statistics begin at the design stage.
Learn more →eTMF — Electronic Trial Master File
Our eTMF gives sponsors and sites a single, always-current view of study documentation.
Learn more →EDC — Electronic Data Capture
We design, build and host electronic data capture systems tailored to each protocol.
Learn more →Clinical Operations
Our clinical operations teams turn protocols into well-run studies.
Learn more →Regulatory Affairs
Regulatory complexity is where many multi-country studies lose time.
Learn more →Our difference
Recruitment is where trials are won — so we built software for it
Enrolment delays are the most common reason studies run late. Our proprietary patient recruitment platform helps us identify the right sites, find eligible patients faster and see enrolment trends in real time.
- Data-led site and country selection
- Live enrolment dashboards for sponsors
- Referral-pipeline tracking and early risk alerts
Why sponsors choose WR Clinicals
- Regional depth: established presence in Eastern Europe, the EAEU and Central Asia
- Experience: 70+ completed trials since 2008
- Integrated technology: EDC, eTMF and recruitment software under one roof
- Accountability: a dedicated project lead for every study
Our network in motion
Sites, patients and data — connected
From Georgia across Eastern Europe, the EAEU and Central Asia, and now to the US: one coordinated team behind every study.
Therapeutic expertise
Experience where it matters to patients
Case studies
How we solve real study challenges
A multi-country device study with a single point of contact
All countries were approved and activated within a coordinated window, with no device-accountability findings.
Family-centred consent in a paediatric study
Retention exceeded the sponsor's expectations throughout follow-up.
Latest insights
Perspectives from our experts
Article
Why patient recruitment fails — and how data-led feasibility fixes it
Most delayed trials are delayed at enrolment. Here is where the plan usually breaks and what to do about it.
Read more →ArticleNavigating EAEU clinical trial requirements: a sponsor's primer
A practical introduction for sponsors planning studies in Eurasian Economic Union member states.
Read more →ArticleInspection-ready from day one: practical eTMF habits
Five habits that keep a trial master file complete, current and ready for inspection.
Read more →Ready to plan your next study?
Tell us about your programme and we will respond with a tailored proposal.