

Accurate statistical analyses and robust datasets
Our team of specialists works in an integrated manner with the clinical, regulatory, and medical writing areas, providing complete support from the study design to the final interpretation of the results, always in compliance with current regulatory guidelines.
Development of clinical and statistical endpoints for study design, in cooperation with medical writing teams
Development of clinical and statistical endpoints for study design, in cooperation with medical writing teams
Sample size calculation, definition of statistical power, and development of randomization schemes
Sample size calculation, definition of statistical power, and development of randomization schemes
Planning and execution of descriptive and inferential statistical analyses
Planning and execution of descriptive and inferential statistical analyses
Development of the Statistical Analysis Plan (SAP), aligned with the study objectives and regulatory requirements.
Development of the Statistical Analysis Plan (SAP), aligned with the study objectives and regulatory requirements.
Preparation of statistical outputs, tables, listings, and figures (TLFs)
Preparation of statistical outputs, tables, listings, and figures (TLFs)
Statistical support for clinical reports and scientific publications
Statistical support for clinical reports and scientific publications
Participation in technical meetings and interactions with regulatory agencies
Participation in technical meetings and interactions with regulatory agencies

A Synvia
Why choose Synvia
More than two decades of experience across the entire drug research and registration chain.
We integrate clinical research, laboratory analyses, and technology to meet the demands of the pharmaceutical industry with quality and global compliance.
CRO Services
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Talk to our experts
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Contact
Talk to our experts
Discover how Synvia can support your studies, analyses, and projects.