- Pharmaceuticals: phase II-IV clinical trials
- Pharmaceuticals: non-interventional studies
- Medical device trials
Data management / Statistics
Data quality is fundamentally important throughout your clinical trial. Only targeted planning at the start of the trial and a valid statistical data analysis will carry your trial to success.
The quality of your data is the starting point for high-quality statistical analysis. Transparent and traceable data enable our data management specialists to perform a solid analysis in your trial.
In close collaboration with our experienced partners, we are happy to support you in all areas of biometrics. Together with you, our qualified data managers strive to develop an efficient and cost-effective strategy for your project.
- Definition of main target criteria
- Sample size calculation
- Randomisation
- Project-specific creation of paper or eCRFs
- Development of databases according to GCP and FDA standards
- Data entry
- Review of the collected data for completeness, consistency and plausibility (validation)
- Statistical analysis
- Interim and final analyses
Data management / Statistics
As your non-interventional study progresses, the quality of your data becomes increasingly significant. Only targeted planning at the start of the trial and a valid data analysis will carry your NIS to success.
The quality of your data is the starting point for high-quality statistical analysis. Transparent and traceable data enables our data management specialists to perform a solid analysis in your non-interventional study.
In close collaboration with our experienced partners, we are happy to support you in all areas of biometrics. Together with you, our qualified data managers strive to develop an efficient and cost-effective solution for your project.
- Definition of main target criteria
- Sample size calculation
- Project-specific creation of paper or eCRFs
- Development of databases according to GCP
- Data entry
- Review of the collected data for completeness, consistency and plausibility (validation)
- Statistical analysis
- Interim and final analyses
Data management / Statistics
It is becoming increasingly necessary to perform clinical trials in order to obtain the CE mark. In this regard, data quality plays a fundamental role. Only targeted planning at the start of the trial and a valid statistical data analysis will carry your trial to success.
The quality of your data is the starting point for high-quality statistical analysis. Transparent and traceable data enable our data management specialists to perform a solid analysis in your trial.
In close collaboration with our experienced partners, we are happy to support you in all areas of biometrics. Together with you, our qualified data managers strive to develop an efficient and cost-effective strategy for your project.
- Definition of main target criteria
- Sample size calculation
- Randomisation
- Project-specific creation of paper or eCRFs
- Development of databases according to GCP and ISO 14155
- Data entry
- Review of the collected data for completeness, consistency and plausibility (validation)
- Statistical analysis
- Interim and final analyses