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Our services

We provide statistical expertise throughout the entire research and development process – from early study design and planning to advanced analysis, modelling and final publication.

Clinical Trials (Phase I–IV)

We provide statistical support throughout the clinical study process according to ICH GCP and EMA and FDA guidelines. With extensive experience in both early phase I studies and large confirmatory phase III trials, we can contribute at all stages of a clinical programme.

  • Study design, endpoint selection and randomisation
  • Simulations, sample size and power calculations
  • Statistical Analysis Plan (SAP)
  • Data cleaning, database lock and quality assurance
  • Analysis programming, TLF production and CSR support
  • DSMB/DMC support and interim analyses
  • CDISC compliance (SDTM/ADaM) and validated analysis datasets
Clinical trials – laboratory research
Register data and real-world evidence – data analysis

Register Data & Real-World Evidence

We help you translate register and health record data into relevant answers to clinical research questions using modern statistical methods and clear analysis. Sweden has internationally unique opportunities for register-based research, and we have extensive experience navigating these data.

  • Cohort and case-control studies
  • Longitudinal models and time-to-event analysis
  • Multiple imputation and missing data handling
  • Propensity score methods, matching and IPTW
  • Data processing, record linkage and control selection
  • Advanced causal inference methods
  • Tables, figures and manuscript support

Clinical Prediction Models

We develop and validate clinical prediction models according to TRIPOD and TRIPOD-AI for clinically applicable and transparently reported models. Our consultants have deep expertise in modelling, calibration and decision analysis.

  • Internal and external validation
  • Calibration, discrimination and decision analysis
  • Bootstrap and cross-validation
  • Development of risk calculators and decision support tools
  • Model implementation and model updating
  • Methods and reporting support prior to publication
Clinical prediction models – statistics and graphs
Statistical consulting – meeting and advisory

Statistical Consulting

We offer flexible advisory services and senior statistical expertise throughout the research process. Whether you need help with a single question or ongoing support throughout an entire project, we are available as your statistical partner.

  • Choice of statistical method and study design
  • Power calculations and advisory before ethics application
  • Research plan and study protocol support
  • Manuscript support, tables, figures and statistical texts
  • Manuscript review, reviewer responses and revisions
  • Support in R, SAS, SPSS and Python

Training

We offer tailored training in statistics and data analysis, adapted to the level and needs of participants. Training can be delivered at your site, at our office or digitally, and can be aimed at anyone from beginners to experienced analysts.

  • Basic and advanced statistics
  • Regression models
  • Survival analysis and competing risks
  • Multiple imputation
  • Longitudinal data, mixed models and GEE
  • Statistics in R, SAS and SPSS
Statistics training – course and teaching

Need statistical support?

Contact us for an initial meeting – we are happy to discuss your project and how we can best assist you.

Contact us