Veristat is a smart, effective and impactful clinical research organization (CRO) that helps biopharmaceutical firms design, build, and run their clinical development programs and navigate the regulatory submission process. Veristat provides experience-based strategic decision-making consulting, the operational efficiencies to manage and monitor international trials, the biometrics expertise to collect, analyze & report clinical trial data to various regulatory agencies, and the therapeutic and medical proficiency to mastermind the entire process. Veristat partners with best-in-class technology solutions to facilitate efficient, cost-effective and quality clinical trial data capture and analysis throughout the clinical development process.

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  • Eastern Europe
  • Europe
  • North America
  • Western Europe

Therapeutic Areas

  • Cardiovascular
  • CNS
  • Dermatology
  • Endocrinology
  • Genetic Diseases
  • Hematology
  • Infectious Diseases
  • Oncology
  • Rare / Orphan Diseases
  • Respiratory
  • Vaccines


Partners are trained on the functionality of the electronic data capture (EDC) and clinical data management (CDM) system, process optimization exercises and scope of Medidata Rave services. This Accreditation teaches the staff to perform end user training, user and site administration, study build, reporting, outputs and amendment manager.