Biostatistics & Programming

At NovoBliss Research®, our Biostatistics and Programming capabilities provide the scientific foundation for robust and reliable clinical evidence. Our experienced biostatisticians offer consultation on trial design, recommend appropriate statistical methodologies, and deliver programming expertise to ensure data accuracy, integrity, and regulatory compliance.

From statistical planning and interim analyses to final study reporting, we apply validated methods and industry-standard tools to generate precise, reproducible outcomes. By integrating scientific rigor with regulatory expectations, NovoBliss Research® enables efficient trial execution and delivers data-driven insights that strengthen claim substantiation and accelerate product development.

Capabilities:

  • Study design consultations & sample‑size calculation

  • Statistical Analysis Plans (SAP) development

  • Randomization scheme generation

  • Interim analyses, futility analyses

  • Integrated summaries of safety & efficacy (ISS / ISE)

  • Programming of Tables, Listings, and Figures (TLFs)

  • CDISC Data standardization & mapping

  • Data cleaning, validation, discrepancy management

  • Statistical reporting & interpretation

  • Expertise with SPSS, R Programming, and GraphPad Prism software