SOCIO- EPIDEMIOLOGICAL STUDIES
OBSERVATIONAL STUDIES / REGISTRIES
CLINICAL TRIALS
Study Design
Clinical Studies Protocol
CRF Design
Informed Consent
Sample Size Calculation
Project Management
Feasibilities
Submissions
Monitoring
Questionnaires Application
eCRF
Data Management Plan
Data Base Development
Data-entry
Data Validation
Queries
Protocol Revision
Statistical Analysis
Statistical Report
Clinical Study Reports
Abstracts
Posters
Papers
Translations
Scientific and Marketing Consulting
Advisory Boards, roundtables
Audits/quality control
Regulatory affairs
Health economics
Programming & Web-Design
Pharmacovigilance
