Versante’s senior personnel have acquired an extensive amount of expertise by managing and contributing to clinical trials related to a substantial list of therapeutic areas.
We can assist with:
Preparation and presentation of development plans
Scientific/medical review of reports
Representation and support at critical meetings with the FDA and other regulatory third parties
Our experts are available for consultation on all aspects of trial design in these therapeutic areas:
Oncology
Cardiovascular
Central Nervous System
Immunology
Vaccine Therapy
Dermatology
Surgical implants
Radio-therapeutics
 
 
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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