Clinical Trial Acceleration

If you’re facing tight research, development, or regulatory timelines, turn to SPRI for clinical trial acceleration. Our team is experienced in meeting our clients’ unique scheduling needs and can help you streamline the enrollment and research process, meeting your deadlines and exceeding your expectations.

Clinical Site Recommendation & Enrollment Services

Learn more about SPRI’s clinical research acceleration capabilities:

  • Site Recommendation – SPRI professionals will assist in the site selection process, focusing on past performance, as well as the clinical site’s level of experience with the therapeutic indication
  • Country Recommendation – After meeting with you to discuss your needs, our team of experts will perform a feasibility assessment and suggest countries based on your internal goals, timelines, patient availability and regulatory requirements
  • Enrollment – Our strategic offices in North America, Eastern Europe, and Western Asia, as well as our partners in Australia, Asia and Western Europe, enable us to expedite clinical trial recruitment and enrollment across the globe

SPRI: International Clinical Trial Performance Experts

From initial feasibility studies and site selection to regulatory management, biostatistics, pharmacovigilance and more, trust SPRI with your next clinical trial. Since 1972, we’ve been the partner biopharmaceutical companies trust for quality, efficiency and local expertise — no matter the size or complexity of the trial.

With strategic offices in the United States (New York and North Carolina), Ukraine, Russia, Georgia and Belarus and strategic partnerships in Western Europe and Australasia, SPRI can easily navigate the challenges of international clinical trials. Contact us today to learn more about our oncology, hepatology, infectious disease, endocrinology and CNS expertise.