Veristat offers Biostatistics and Programming services



Biostatistics

Veristat biostatisticians and SAS programmers apply scientific principles as well as indication-specific knowledge to study design, protocol sample size and endpoint development, creation of analysis plans, SAS programming, and statistical analyses.

Biostatistics and Programming services include:

  • Study design / protocol development
  • Statistical consulting
  • Sample size calculations
  • Randomization schemes
  • Statistical analysis plans
  • Protocol and CRF review
  • Statistical programming using SAS
  • Data conversion
  • Statistical tables, data listings, and figures for clinical study reports (CSRs)
  • Statistical analyses and reports
  • Pharmacokinetic and pharmacodynamic analyses
  • Statistical representation at FDA meetings
  • Integrated safety and efficacy analyses (ISS/ISE/CTD)
  • Data Monitoring Committee services
  • CDISC-compliant datasets
 
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ABOUT VERISTAT

Veristat is an independently owned clinical research organization (CRO) located just outside of Boston. The company was founded in 1994 by John Balser, PhD, and Barbara Balser, VMD, with the intent of providing high-level statistical and medical consulting services to the pharmaceutical and biotechnology industries. Today, Veristat has steadily grown to over 78 experienced employees, providing comprehensive clinical and analytical research services. However, Veristat remains a relatively small company by design, enabling the company's principal staff to continue to work closely with our clients on an individualized basis.

Our clients range from small to large global companies, engaged in the development of new pharmaceutical and biological products, vaccines, medical devices, and diagnostic agents. Veristats client base has progressively grown largely based on industry referrals and the companys commitment to client-focused services.