Plan your study
Settle the question, design and sample size before the first participant or record.
Biostatistics for clinical research
Statistics that hold up to peer review
We design, analyse and defend the numbers behind clinical studies — with a pre-agreed plan, reproducible code and a written record of every decision.
NDA first · plan agreed first · code handed over
Live analysisHypothetical data
Adjusted odds ratios · 95% CI
Atopic history2.4 (1.5–3.9)
Male sex1.8 (1.1–2.9)
PPI use1.3 (0.8–2.1)
Age, per 10 y0.9 (0.7–1.2)
Intervals crossing 1 are reported as such — never rounded into significance.
Work delivered for researchers at academic medical centers in
- United States
- Europe
- Middle East
- Asia
Selected engagement · Gastroenterology
Which factors were associated with eosinophilic esophagitis?
For a US academic medical center, we worked with a case-control dataset, checked how the data were handled and used multivariable logistic regression to estimate associations.
- Design
- Case-control
- Method
- Multivariable logistic regression
- Deliverable
- A statistical analysis report prepared for publication
Study support
Support at each stage of a study
Start where you are. Each service has a defined scope and deliverable, agreed in a written proposal before any work begins.
Analyse your data
Check the dataset, run the pre-agreed analysis and understand what the results can support.
Prepare for publication
Report methods and results clearly, verify them independently and answer reviewers.
Engagement process
How an engagement works
Every project follows a structured, documented process — from initial scoping through final delivery — with confidentiality and reproducibility built in at every stage.
Discuss your study01Project scoping
No data shared yetSubmit project details. We confirm study type, objectives, data status, and timeline. No files are transferred at this stage.
02Confidentiality agreement
NDA firstNDA executed before any data or materials are shared. All content is handled under confidentiality for the lifetime of the engagement.
03Statistical analysis plan
Pre-specifiedPre-specified SAP drafted collaboratively and approved before analysis begins. Defines endpoints, methods, populations, and missing data handling.
04Analysis and documentation
ReproducibleAnalysis executed in a reproducible environment following the pre-specified SAP. Outputs logged with software versions.
05Reporting and delivery
Full packagePublication-ready report with tables, figures, and methodology narrative. Full package: analysis code, data dictionary, and audit trail.
Free library
Tools and guides you can use today
Free to use, no account needed. They are planning aids, not a substitute for statistical review of your study.
Interactive tools
Calculators and planning aids that run in your browser, for the decisions between an idea and a report.
Open the Research WorkbenchPractical guides
Worked explanations of the decisions that reviewers and statisticians ask about.
- Understanding sample size calculation in clinical trials
- Common statistical errors in medical manuscripts
- The reviewer asked: explain your missing data
Worksheets and templates
Editable planning documents, checklists and curated links to official sources.
See all resourcesAbout
A statistical consultancy for medical research
StatMedAnalysis provides expert biostatistics consulting and statistical support to healthcare researchers and institutions globally. We work across the full research lifecycle — from protocol design through regulatory submission and publication.
Our focus is collaborative, rigorous work that meets the standards expected by leading medical journals, funding agencies, and regulatory bodies.
Engagements completed for researchers at academic medical centers in the United States, Europe, Middle East, and Asia.
Statistical work delivered across gastroenterology, ophthalmology, and related clinical research specialties.
Analytical deliverables aligned with CONSORT, STROBE, and observational study reporting standards.
Statistical precision
Every analysis follows a pre-specified plan. Methods are chosen to match the study design, not the desired result.
Data confidentiality
NDA executed before data transfer. Strict access controls, secure handling, and research-data retention governed by each project agreement.
Scientific rigor
Rigorous, reproducible workflows with full audit trails — suitable for regulatory submission and peer review.
Timely delivery
Realistic timelines set at scoping. Milestone communication throughout. Expedited options for urgent deadlines.
Start a project
Tell us about your study
Describe your research project and we'll acknowledge your inquiry within 24 hours and follow up with a scoped proposal within 3 business days. Prefer email? support@statmedanalysis.com
Contact information
Response Time: Acknowledgment within 24 hours
Global Service: All time zones supported
Language: English
Engagement process
- 1.Submit project details via the form
- 2.Acknowledgment within 24 hrs · Proposal within 3 business days
- 3.Review and approve the Statistical Analysis Plan
- 4.Receive analysis, report, and reproducible documentation
All engagements are covered by a non-disclosure agreement. Data is handled securely and returned with full audit documentation.
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