Statistical
Consulting & Programming
Esculape and DATAN – joining forces in statistics and data management
Through our strategic partnership with DATAN, a Münster-based full-service provider with more than 35 years of experience in statistical consulting. programming and data analysis we are expanding our serive portfolio with an experienced team of statistical expersts.
This enables us to support you even more comrehensively thorughout the entire clinical trial process - from study planning thorugh to submission-ready analyses.
Statistical Consulting
In-depth expertise for every statisctical challenge
DATAN provides professional, practice-oriented consulting across all statistical aspects of clinical trials – from sample size planning to the final analysis methodology. Quality, speed and flexibility are at the heart of our approach, enabling even complex study designs to be implemented on schedule and in close collaboration with the client.
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Study and analysis planning, including Statistical Analysis Plans (SAPs)
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Sample size planning and estimation
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Complex modelling and simulations
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Consulting on data collection and study design
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Interpretation and quality assurance of analysis results
Statistical Programming
Submission-ready results to the highest standards
DATAN’s programming team consists of statistical programmers with extensive experience in both SAS® and R who have contributed to clinical trials across a wide range of phases and study sizes.
By consistently adhering to industry standards and making effective use of relevant innovations, DATAN ensures that every project is implemented in accordance with the applicable requirements and specifications.
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Development and validation of datasets for clinical study reports
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Implementation according to sponsor-specific or CDISC standards, including ADaM
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Generation of validated, submission-ready outputs
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Implementation within client systems or DATAN’s own IT infrastructure
DMC Management Services
Independent statistical support for Data Monitoring Committees
DATAN provides independent statistical DMC services as well as SAC analyses for clinical trials, acting as a neutral partner to help safeguard patient safety and study integrity throughout the course of a study.
Real World Daten & Real World Evidenz
Robust insights from clinical practice
To support evidence-based decision-making throughout the entire pharmaceutical product lifecycle, DATAN assists with the analysis and interpretation of real-world data, complementing evidence generated from traditional clinical trials.
DATAN AI+ – AI-Powered Automation for Clinical Trials
Greater efficiency through AI – GDPR-compliant and hosted in the EU
With DATAN AI+, DATAN also provides an AI-powered platform alongside dedicated consulting and training services for clinical trial teams.
Services range from process consulting and AI vendor selection to training programmes and prompt engineering tailored to the life sciences sector. This enables recurring, document-intensive tasks to be completed significantly faster while maintaining the highest standards of data security.

