SPRI is the premier Eastern European full-service CRO. We help clients meet the challenges of managing global clinical studies, regardless of size or complexity. Our experienced staff can seamlessly manage your clinical study from strategically-placed offices in Eastern Europe and the United States.
SPRI facilitates communication among investigators, the Sponsor and other parties, while never losing focus of the specific tasks assigned to them.
Our positive workplace environment and tremendous growth opportunities makes SPRI's staff turnover extraordinarily low. SPRl's management team has years of site level experience and a true under-standing of issues such as recruitment, CRF completion and query resolution.
Strong Feasibility Assessment resulting in evidence-based site recommedation
High Costs
Faster enrollment accelerates timelines
Clinical Staff
Investment in employee development
Regulatory Hurdles
Strategic country selection partnered with strong regulatory expertise
Logistical Hurdles
Fulltime logistical staff with proactive approach
Data Quality
Qualified site staff, comprehensive site training and meticulous oversight
Patient enrollment difficulties...
are the leading cause of time delays in clinical trials
Time-to-market is the critical ROI driver in clinical stage compounds. For a new efficacious drug, the completion cost for multi-phase clinical trials is directly proportional to the duration.*
Solution: Run clinical sub-trials where patient recruitment is fastest.
SPRI has infrastructure in several American and European locations, with largely untapped populations.
