Biostatistics and Statistical Programming

Clinovo is your complete source for comprehensive biometrics solutions designed to ensure your clinical trial data is held with highest data security standards as per ISO/IEC 27001. Our Biostatistics and Statistical Programming team provide full-service support through all phases of clinical development and commercialization. Our expert biostatisticians and statistical programmers are located globally and trained in current methods and standards to support the successful execution of your projects. We have built a reputation as a preferred partner for our clients around the world by providing superior solutions that reduce complexities and speed up time to market for your products. With Clinovo, You get more than just data analysis – you get a real, deep understanding of modern biometrics and the drug development.

Services We Offer:

  • Study design and protocol development
  • Sample size estimation
  • Statistical analysis plans
  • CDISC-compliant datasets and documentation (SDTM/ADaM)
  • Statistical reports generation
  • Submissions readiness
  • CSR review
  • Integrated summaries (ISS/ISE) for regulatory submission
  • Exploratory analyses
  • DSUR’s
  • PSUR’s
  • RMP analysis
  • Publications support

Let’s Accelerate Clinical Development Together! Contact Us >>

Clinovo is your complete source for comprehensive biometrics solutions designed to ensure your clinical trial data is held with highest data security standards as per ISO/IEC 27001. Our Biostatistics and Statistical Programming team provide full-service support through all phases of clinical development and commercialization. Our expert biostatisticians and statistical programmers are located globally and trained in current methods and standards to support the successful execution of your projects. We have built a reputation as a preferred partner for our clients around the world by providing superior solutions that reduce complexities and speed up time to market for your products. With Clinovo, You get more than just data analysis – you get a real, deep understanding of modern biometrics and the drug development.

Services We Offer:

  • Study design and protocol development
  • Sample size estimation
  • Statistical analysis plans
  • CDISC-compliant datasets and documentation (SDTM/ADaM)
  • Statistical reports generation
  • Submissions readiness
  • CSR review
  • Integrated summaries (ISS/ISE) for regulatory submission
  • Exploratory analyses
  • DSUR’s
  • PSUR’s
  • RMP analysis
  • Publications support

Let’s Accelerate Clinical Development Together! Contact Us >>

Let’s Connect!