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Let Our Family Care for Your Family!

Benefits of Cardiovascular Strategic Site Network

Site Capabilities

  • -20°C Freezer
  • Central IRB
  • Electronic medical records
  • IVUS
  • 1-2 Full-time CRC's
  • QCA
  • 1 monitoring location

Centralized Study Start-Up

  • One regulatory package sent to SCRI
  • SCRI centrally completes all regulatory documents
  • SCRI manages all central IRB submissions

Centralized Clinical Trial Agreements (CTAs)

  • SCRI negotiates the CTA on behalf of the site
  • All CTAs are 3-party agreements between the site, SCRI and the Sponsor/CRO
  • All payments are made directly to SCRI who then pays each of the sites

QA Oversight

SCRI conducts quarterly on-site audits of all strategic sites

Marketing and Patient Recruitment

SCRI provides dedicated, full-time marketing and patient recruitment professionals

Clinical Oversight

SCRI provides clinical oversight for strategic sites via physician leadership and dedicated clinical operations staff

Scientific and Investigator-Initiated Resources

SCRI Research Consortium provides Sponsor support to SCRI research Investigators for creation and implementation of clinical trials