A Full-Service Clinical Research Organization

PROMETRIKA delivers highly streamlined and tailored services for very specific needs at any stage in a clinical research program, including:

  • Stand-alone database build and User Acceptance Testing (UAT)
  • Phase 1 data management, analysis and reporting, including PK/PD analyses
  • CDISC SDTM conversion programming to generate submission-ready datasets accompanied by the required documentation
  • Comprehensive support of Independent Data Monitoring Committees (IDMC), independent adjudication committees, clinical event committees
  • Independent validation of SAS® programs
  • Adaptive clinical trial design
  • Stability analyses for drug expiration dating
  • Statistical validation of centralized randomization via IVRS
  • Randomization call center services
  • Phase 4 support, including exploratory analyses and editorial services related to abstracts, posters, manuscripts, and scientific meeting presentations

Internet Explorer has detected you are viewing this page in Compatibility View. PROMETRIKA.COM works best if you turn this off.


Please change to normal view by clicking on Tools and then Compatibility View