Description
Networld Online’s IRB Clinical Study Research Program Set Up is a comprehensive one-time onboarding service that establishes all foundational systems, documentation, and processes needed for your medical practice to begin conducting IRB-compliant clinical research studies. Our team of research specialists works directly with your staff to configure your research infrastructure for long-term study success.
What’s included:
- Initial IRB application preparation and submission
- Research site assessment and compliance gap analysis
- Protocol and consent form development
- Staff training on IRB requirements and research procedures
- Data management system setup and configuration
- Regulatory binder creation and document organization
