Rapid protocol development

• Dedicated development staff facilitate final protocol throughout various levels of scientific, statistical, and operational review.

Rapid contracting

• HCRN negotiates study funding agreement with lead institutions and companies providing study support.
• HCRN expedites site contracting by executing work orders under a master agreement with member institutions.

Rapid site activation

• HCRN maintains baseline general regulatory documents (e.g., CVs, medical licenses, laboratory certifications, etc.).
• Dedicated regulatory staff coordinate documentation for timely site-specific IRB submission.
• Dedicated project managers coordinate web-based training, SIVs, and comprehensive study management.