TRIAL PLANNING
A scientifically sound planning of a clinical trial is essential for its successful conduct. Together with our well qualified partners we offer the following planning services:
- Contract administration
- Development of trial designs
-
Protocol development
- Sample size estimation
- Development of the Statistical Analysis Plan (SAP)
- Development of an Informed Consent Form (ICF) and patient information

- Case Report Form (CRF) generations
- Development of a data management plan
- Development of trial procedure manuals and project plans
- Development of monitoring plans
- Generation of randomization schedule
- Patient insurance
- Investigators meeting
- Contract administration
- Development of trial designs
- Protocol development
- Sample size estimation
- Development of the Statistical Analysis Plan (SAP)
- Development of an Informed Consent Form (ICF) and patient information

- Case Report Form (CRF) generations
- Development of a data management plan
- Development of trial procedure manuals and project plans
- Development of monitoring plans
- Generation of randomization schedule
- Patient insurance
- Investigators meeting