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  Institute Twain

Statistical Programming in Clinical Research



 
 

 

Preclinical research


Support in the phase 0 and in the phase 1:
• Experiments with microdoses
• Recommended dose of the molecule for the design and clinical research
• Toxicity and its restriction of the dose (dose limiting toxic effect, DLT)
• Effects of the pharmacokinetics and pharmacodynamics of the molecule
• Determination of healing effect

 

 

Clinical research, pharma


Support in the phase 2, phase 3 and later:
• experimental design, planning the study and the protocols
• adaptive methods
• ensuring the reproducibility and transparency
• biomarkers
• streamlining clinical trials

 

 

 

 

 

 

 

   

Institute Twain: the most favourable institute for statistical programming and statistical consulting in Germany