Our Services

Specialized biostatistics and programming services for Phase 1 clinical trials and early drug development

Phase 1 Clinical Trial Expertise

Specialized in early phase clinical trials and first-in-human studies

Biostatistics
Expert statistical analysis for early phase trials
  • Phase 1 trial design and analysis
  • Sample size and power calculations
  • Dose escalation methodologies
  • Safety data analysis
  • Interim analyses for early decisions
  • DSMB and IDMC support
Statistical Programming
Cutting-edge R and Python programming
  • Validated R and Python environments
  • CDISC SDTM and ADaM datasets
  • Custom analysis workflows
  • PK/PD data processing
  • Safety data automation
  • Reproducible reporting
Early Drug Development
Comprehensive early phase support
  • First-in-human study design
  • Dose escalation strategies
  • PK/PD modeling support
  • Safety analysis expertise
  • Regulatory submission support
  • IND submission assistance

Need Phase 1 Trial Support?

Contact our team today to discuss how ClinPharmStats can support your early phase clinical trials.

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