

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.
Clinical and statistical endpoints in cooperation with medical writing
Clinical and statistical endpoints in cooperation with medical writing
Sample size calculation, statistical power, and randomization
Sample size calculation, statistical power, and randomization
Descriptive and inferential statistical analyses
Descriptive and inferential statistical analyses
Statistical Analysis Plan (SAP) aligned with regulatory requirements
Statistical Analysis Plan (SAP) aligned with regulatory requirements
Statistical outputs, tables, listings, and figures (TLFs)
Statistical outputs, tables, listings, and figures (TLFs)
Support for clinical reports and scientific publications
Support for clinical reports and scientific publications
Technical meetings and interactions with regulatory agencies
Technical meetings and interactions with regulatory agencies


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
Other solutions
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Contact
Talk to our experts
Discover how Synvia can support your studies, analyses, and projects.

Contact
Talk to our experts
Discover how Synvia can support your studies, analyses, and projects.