Bio Statistical Services

Our statisticians design studies, calculate sample sizes, and analyze trial data to determine whether your treatment works.

Overview

Statistics is where you prove your drug works. We write statistical analysis plans that define exactly how the data will be analyzed, run power calculations to make sure you enroll enough patients, and perform the statistical tests that go into your regulatory submission. All our analyses are done in SAS with full documentation and quality checks.

Biostatistical analysis and data modeling

What We Do

Writing statistical analysis plans that specify endpoints, populations, and analysis methods

Performing sample size calculations and power analyses for trial planning

Running statistical analyses using SAS including ANCOVA, survival analysis, and mixed models

Conducting interim analyses for data monitoring committees with appropriate alpha spending

Creating tables, listings, and figures for clinical study reports and submission packages

Why Work With Us

Our biostatisticians have PhDs in statistics with 15+ years in clinical trials

We follow CDISC standards for datasets and use validated SAS macros

Independent statistical review catches errors before data goes to regulators

Related Services

Clinical Data Management

EDC systems and data quality control

Medical Writing

Regulatory documents and study reports

Bioavailability and Bioequivalence (BA/BE)

BA/BE studies for generic drug approvals

Clinical Development Services

Phase I-IV trial management

Ready to Get Started?

Let's discuss how we can support your bio statistical services needs.