ICRC-WEYER provides comprehensive biometric services for all phases of clinical research and across a wide range of therapeutic areas. The experience of our biometrics team ranges from phase I first-in-man and pharmacokinetic trials to large observational studies.

Whether your study requires standard statistical analyses or involves complex methodological issues, we are committed to develop customised solutions which meet your research goals.

We have expertise in developing, validating and applying biometric tools within a variety of study designs and statistical approaches. ICRC-WEYER’s biometric experts have developed validated SAS macros for the calculation of pharmacokinetic parameters and host an extensive library of SAS programs and macros.

Due to seamless integration with our in-house Data Management and Medical Writing departments as well as with our associated medical experts, we have developed harmonised and efficient work processes from database set-up to reporting of analysis results. Therefore ICRC-WEYER can offer you fully-integrated biometric solutions adhering to your time and cost frame.

The CDISC ADaM-Standard is now available. 

Statistical consulting:

• Sample size estimation and power calculation
• Statistical consulting regarding study design and study protocol

Biostatistical planning and analysis:

• Statistical analysis plan
• Randomisation
• Statistical evaluation (phase I – IV clinical studies, data overviews, interim-analysis, meta-analyses)
• Pharmacokinetic analysis
• Pharmacodynamic analysis
• Report preparation

Statistical programming:

• Presentation of analysis results supported by comprehensive tables, figures and data listings
• Periodic review of programming standards

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