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"Medistat" Ltd. offers the following services to clients engaged in pre-clinical, PK/PD, phase I-IV, and post-marketing clinical studies:
 
 

Statistical Consulting

  • Development of Protocol
  • Experimental Design
  • Interim Analysis
  • Sample Size and Power Calculation
  • Statistical Analysis Plan Meta Analysis
  • Statistical Related Regulatory Issues

Data Management and Data Bases

  • Data Logging and Data Collation
  • Data Query and Resolution
  • CRF Design and Development
  • Databases Design
  • Data Transfer/Transport
  • Data Entry
  • Data Verification

 

Statistical Programming

  • SAS® Programming for Standard and Special Statistical Analysis
  • SAS® Programming for Summary, Efficacy and Safety Tables
  • SPSS® Programming for Standard and Special Statistical Analysis
  • SPSS® Programming for Summary, Efficacy and Safety Tables

 

Statistical Reporting

  • Interpretation of Statistical Outputs and Results
  • Integrated and Stand Alone Statistical reports
  • Electronic Documents Integration
  • Preparation of Regulatory Submission

Services: Clinical Trial Design, Data Management, Health Economics, Pharmacoeconomic Studies, Pharmacoepidemiology Studies, Programming: Database/SAS/etc, Quality Assurance / Control, Quality of Life Assessment, Data Entry,