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WE AT ASSIGN UNDERSTAND THAT PROFOUND PLANNING OF THE
DESIGN OF CLINICAL STUDIES AND A SOUND DATA ANALYSIS IS THE KEY
TO RELIABLE CLINICAL STUDY RESULTS. WE PROVIDE STATISTICAL APPROACHES THAT ARE CUSTOMIZED TO THE OBJECTIVES OF YOUR
CLINICAL STUDY.

We have the in-depth expertise and experience of 20 years of designing the
biostatistical parts of clinical development programs.

We have strong therapeutic experience in various indications from oncology
to vaccines and in a wide range of statistical methods.

OUR CAPABILITIES INCLUDE:

– Study design phase I - IV
– Sample size calculations
– Statistical methods applications
– Review of entire protocols and statistical parts
– Randomizations
– Statistical programming, e.g. descriptive statistics and univariate analysis,
   linear and nonlinear models, categorical data analysis
– Interim analyses
– Statistical Analysis Plans
– Statistical programming (SAS®)
– Integrated safety and efficacy analysis
– Clinical study reports: tables, figure, listings, bookmarked and hyperlinked