Our expertise is unparalleled in the industry. We support you by improving your effort to evaluate the efficacy and safety of drugs through the proper planning of, and excellent research approach to, the clinical trials and protocols. We also focus on optimum data collection, management and analysis methods, so you can go to market ahead of your competition. Our commitment to quality ensures the very best service for you.
To learn more about our services please select one of the categories on the right or contact us at info@versanteintl.com.
Versante Service Areas:
Strategic Leadership for Drug Development Plans
Protocol Development
Development of Statistical Analysis Plans
Preparation of Randomization Schedules
Clinical Data Management
Statistical Analysis
Statistical Programming Using SAS™
Regulatory Submissions of Electronic Data
Report Writing
 
 
Statistical Analysis and Reporting
Biometrics
Clinical Plan Development
Protocol Development and Study Design
Therapeutic Expertise Consultation
Data Management
Electronic Data Capture (EDC)
CDISC Conversion
 
 
 
 
 
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