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:

  1. Contract administration

  1. Development of trial designs

  1. Protocol development

  1. Sample size estimation

  1. Development of the Statistical Analysis Plan (SAP)

  1. Development of an Informed Consent Form (ICF) and patient information

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  1. Case Report Form (CRF) generations

  1. Development of a data management plan

  1. Development of trial procedure manuals and project plans

  1. Development of monitoring plans

  1. Generation of randomization schedule

  1. Patient insurance

  1. Investigators meeting