FAQ

Frequently Asked Questions

Quickly learn about EvoClinical through these frequently asked questions. 

EvoClinical is a specialized consulting firm providing statistical analysis and data management for life science companies running clinical trials. We help sponsors design, analyze, interpret clinical studies and manage data with expert guidance to ensure data integrity, regulatory compliance, and successful trial outcomes.

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EvoClinical offers a full range of statistical and data management services for clinical trials, including study design consulting, protocol development support, statistical analysis planning, data management oversight, preparation of TFLs (Tables, Figures, Listings), regulatory support, medical writing and training in clinical research statistics.

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Unlike full-service CROs, EvoClinical focuses exclusively on biostatistics and data expertise. We provide senior-level statistical leadership, ensuring sponsors receive expert-driven guidance without the overhead of unrelated services.

Why clients choose EvoClinical >

EvoClinical partners with pharmaceutical companies, biotechnology firms, medical device manufacturers, and CROs. Our clients range from small startups needing statistical leadership to global enterprises requiring specialized support.

EvoClinical provides regulatory support services, including preparing statistical data packages, generating TFLs, drafting briefing documents, and supporting sponsor teams during FDA, EMA, and Health Canada meetings. We do not file regulatory applications but ensure all statistical elements are accurate, defensible, and regulator-ready.

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Yes. EvoClinical uses advanced feasibility tools to analyze trial landscapes, assess similar study designs, identify investigators and sites, and predict enrollment timelines—helping sponsors plan more accurate and competitive trial strategies.

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Yes. EvoClinical provides custom statistical analysis training for teams. Training covers protocol interpretation, study design features, hypothesis testing, missing data methods, and results interpretation, helping staff better engage with trial data.

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Partner with a CRO you can trust.

Our process helps put you at ease when purchasing statistical services for your clinical trial needs.

We’re happy to answer any questions you may have and help you determine which of our services best fit your needs.

Our client focus:
What happens next?
1

Schedule a call

2

Discovery Conversation 

3

We prepare a proposal 

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