Statistics Services

Trionfo Research's statistics department operates globally, providing data and expertise to facilitate faster, more informed decisions. Our team offers reliable and flexible services, working closely with the data management team to deliver integrated and seamless data solutions. Whether you need full-service studies or a strategic bespoke solution, we can tailor our services to meet your organization's needs.
Our biostatistics team has extensive experience in designing and analyzing clinical trials across a wide range of therapeutic areas. We offer solutions tailored to your requirements, including Phase I-IV Clinical Trials, Late Phase/Real World studies, Regulatory Submissions, as well as complex surveys and longitudinal studies.
At Trionfo Research, we are committed to providing high-quality statistical support to help you achieve your research goals. Our team is dedicated to delivering innovative and reliable solutions that meet the highest standards of quality and accuracy.

Our Solutions and Expert Staff

Trionfo Research provides comprehensive support for clinical trials and research projects from inception to publication. Our analyses are conducted using up-to-date and validated software, such as SAS and Stata for statistical analyses, PASS for sample size calculations, and nQuery, adhering to ICH GCP standards with a focus on validation, traceability, and reproducibility.
Our team of statistics experts at Trionfo Research is experienced in analyzing and designing clinical trials across various therapeutic areas. Some of the areas we specialize in include, but are not limited to: Oncology, Cardiology, Neurology, Respiratory, Nephrology, Endocrinology, Pain Control, Infectious Diseases, Critical Care, Substance Abuse, and a variety of Medical Devices.
From planning and design to analysis and reporting, Trionfo Research is dedicated to ensuring that your research projects are conducted with the highest standards of quality and compliance.

Trionfo Research biostatistics department’s key outputs include:

  • Study design and protocol review
  • Sample size and power calculations
  • Randomization
  • Statistical analysis plan
  • Adaptive trial design
  • Biostatistics consulting services
  • Feasibility analysis
  • CDISC (SDTM and ADaM)
  • Data Safety Monitoring Board (DSMB) support
  • Interim analyses
  • Statistical analysis/TLF production
  • Independent/unblinded analyses and support
  • CSR input
  • Narratives Programming
  • Patient profiles
  • Data conversion and integration
  • Submission strategy, planning, and analyses
  • Post-marketing manuscript support
  • Pharmacoeconomics
  • Late phase solutions