SERVICES
Services
Patient-Centric
Evidence Development
Clinical Research Management
for sponsors/CROs
Clinical Investigator Support
and Site Management
Education and Training
Society Presentations
and Publications
Education and Training
- Infrastructure and Resource Support for Evidence Collection
- Good Clinical Practice Training
- Tips for Publishing Patient Reported Outcome Data
- Best Practice for Subject Recruitment
- Best Practice for Subject Retention and Compliance
- Protocol Development
- Institutional Review Board Processes
- U.S. Regulation Training for Biologics, Investigational New Drugs, and Investigational Device Exemptions
- Provide Research Responsibility Training for the Following Roles:
- Principal Investigators
- Sub-Investigators
- Study Coordinators
- Trial Managers
- Administrative Assistants
- Recruitment Specialists
- Regulatory Associates/Coordinators
- Site Managers
- Clinical Research Associates/Monitors