For health researchers and clinical study teams

Clinical and Health Data Analysis

Journals, ethics boards and funders all ask the same question: is the analysis sound? We provide statistical analysis for clinical and health research, including observational studies, trial analysis, occupational health surveys and health program data. Every analysis follows recognized reporting guidelines, so your results are ready for peer review.

SURVIVAL CURVESTreatmentControlHAZARD RATIOSAge 65+WomenDiabetesOverallHR = 1Sample data for illustration
Best forHealth researchers and study teams
MethodsSurvival, regression, diagnostic accuracy
GuidelinesCONSORT and STROBE aware reporting
ToolsR, Stata, SPSS

The short answer

What does clinical data analysis include?

Clinical and health data analysis applies biostatistics to research questions about patients, treatments and health outcomes. Typical work includes comparing groups, modeling risk, analyzing time to event outcomes and assessing how well a test detects disease.

Reporting matters as much as method. Journals expect analyses to follow guidelines such as CONSORT for randomised trials and STROBE for observational studies.

Study timeline

Where clinical data analysis fits in your research cycle

Clinical and health research has strict stages, from protocol to publication. Statistical choices made before data collection decide what a study can show, so we are involved from the protocol and carry the analysis through to the paper.

Month 1Month 6Month 12Month 18Protocolanalysis planEthics approvalstats sectionData collectionform reviewData managementinterim checksAnalysisfull analysisPublicationreviewer repliesStudy activityStatistician involvementIllustrative 18 month timeline

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01
Protocol

Clinical lead

Their workWrites the research question and study design.
How we helpSets the primary outcome, sample size and analysis plan before data is collected.
02
Ethics approval

Ethics committee

Their workReviews the protocol and consent process.
How we helpProvides the statistical sections the committee needs, including the privacy approach.
03
Data collection

Clinical staff

Their workRecords patient or participant data.
How we helpAdvises on data forms and coding, so the data can be analyzed as planned.
04
Data management

Data manager

Their workCleans, codes and locks the study data.
How we helpRuns checks for missing, impossible or inconsistent values and documents them.
05
Analysis

Statistician

Their workRuns the planned analysis and sensitivity checks.
How we helpRuns the analysis in R or SPSS, with confidence intervals and assumptions checked.
06
Publication

Research team and journal

Their workWrites and submits the manuscript.
How we helpWrites the methods and statistics sections and responds to reviewer comments.

Who it is for

Built for teams like yours.

01

Clinical researchers

Analysis and statistical sections for papers, theses and conference abstracts.

02

Public health teams

Survey and surveillance data analysis for reports and policy.

03

Occupational health studies

Exposure, risk and outcome analysis for workplace health research.

What you get

Clear deliverables, agreed up front.

Analysis that stands up to peer review. Every project is quoted as a fixed price after a free assessment, so you know the cost before work begins.

  • A statistical analysis plan
  • Descriptive tables (Table 1) and group comparisons
  • Regression, survival or diagnostic accuracy analysis
  • Journal quality figures such as Kaplan Meier curves and forest plots
  • A statistical methods section draft for your review
  • Reproducible R, Stata or SPSS code

Packages and pricing

Pick the depth you need.

Starting prices are shown for each option. Your final price is a fixed quote, agreed after a free assessment of your data and scope, so there are no surprises.

Before data collection

Study Planning

The statistical foundation reviewers and ethics boards expect.

From $400fixed project
  • Sample size and power calculation
  • Statistical analysis plan
  • Statistical section for the protocol
Get a fixed quote
Recommended for most studies

Full Analysis

The complete analysis, carried out as planned and clearly reported.

From $1,200fixed project
  • Everything in Study Planning
  • Data checks and coding review
  • Primary and secondary analyses
  • Tables, figures and methods text
  • R or SPSS code
Get a fixed quote
After submission

Publication Support

Help with statistical reviewer comments and extra analyses.

From $300fixed project
  • Response to statistical comments
  • Additional analyses requested
  • Revised tables and text
Get a fixed quote

How it works

Four steps from question to answer.

  1. Step 1

    Protocol review

    We review your study design, outcomes and sample size.

  2. Step 2

    Analysis plan

    We agree methods before touching the results.

  3. Step 3

    Analysis

    We run and check the analysis, testing assumptions.

  4. Step 4

    Reporting

    You receive tables, figures, methods text and code.

Questions we help you answer

If you are asking these, we can help.

Sample size and powerLogistic and Cox regressionKaplan Meier survival analysisSensitivity, specificity and ROC curvesConfounding and adjustmentRepeated measuresCONSORT and STROBE reporting

Tools we use

RStataSPSSExcel
  • ?Does the treatment group survive longer?
  • ?Which risk factors predict the outcome?
  • ?How accurate is this diagnostic test?
  • ?Is our sample size adequate?
  • ?How do we adjust for confounders?
  • ?What should go in our methods section?

FAQ

Questions about Clinical and Health Data Analysis

Cannot see your question? Ask it in the enquiry form and you will get a direct answer.

See all FAQs
Do you support regulatory submissions?

Our focus is research analysis for publication, theses, grants and program reports. Regulatory submissions to agencies such as the FDA require specialised standards, and we will tell you honestly if your project needs a dedicated regulatory team.

Can you calculate sample size for my study?

Yes. We calculate sample size and power for your primary outcome and design, with a short justification you can include in protocols and ethics applications.

Can you write the statistical methods section?

We draft the statistical methods text describing what was done, for you and your coauthors to review and own.

How is patient data protected?

We work only with de identified data, share files through secure links and delete data on request after delivery. We can sign confidentiality agreements.

Can you respond to reviewer comments?

Yes. We help address statistical reviewer comments, including extra analyses and clear written responses.

Our services

All eleven services

Services overview
AI, automation and coaching

Statistics Coaching

View service Research and survey analytics

Survey Analytics

View service Research and survey analytics

Survey Design and Questionnaires

View service Data quality and business intelligence

Data Cleaning and Validation

View service Research and survey analytics

Monitoring and Evaluation

View service Data quality and business intelligence

Business Intelligence and Dashboards

View service Data quality and business intelligence

Product Insight Review

View service Data quality and business intelligence

Statistical Process Control

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Clinical and Health Data Analysis

AI, automation and coaching

Data Automation and Web Data Collection

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AI Automation and Chatbots

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Tell us about your data. We will tell you what it can answer.

Send a short description and receive a free assessment with a suggested approach, timeline and fixed quote.

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