Your trial data matterS

With three decades of experience, we focus on your trial outcome. As data experts, we work in your trial with the end in mind.

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Central, technology-enabled, full-service study management

  • Development Consulting
  • Project Management
  • Clinical Monitoring
  • Data Management & Biostatistics
  • Own eClinical EDC & CTMS Solution Vitessa
  • FSP and Personal Leasing

Broad experience, including:

  • Medical device and IVD studies
  • Early development expertise
  • Regional and global post-marketing trials
  • Data integration, warehousing and submission readiness

Biometrical excellence since 1991

  • FSP in Biostatistics & SAS Programming
  • Statistical consulting 
  • Contribution to study design
  • Power analysis and sample size calculation
  • Randomization
  • Statistical analysis plans
  • Periodic data monitoring and safety reviews
  • Statistical modelling, analysis, reports and publication
  • HEOR including HTA

KOEHLER eClinical is proud to be a member of: