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    • Home
    • About
      • Team of Experts
      • Operations Team
    • Areas of Expertise
    • Services
      • Global Regulatory Affairs
      • Global Quality Compliance
      • Global Clinical Affairs
      • Clinical Operations
      • Medical Affairs
      • Inspection Readiness
      • FDA Correspondent
      • M&A / Divestiture
      • Program Management
      • Training
    • Resources
      • Webinars
      • Blog
      • News
    • Contact Us
  • Home
  • About
    • Team of Experts
    • Operations Team
  • Areas of Expertise
  • Services
    • Global Regulatory Affairs
    • Global Quality Compliance
    • Global Clinical Affairs
    • Clinical Operations
    • Medical Affairs
    • Inspection Readiness
    • FDA Correspondent
    • M&A / Divestiture
    • Program Management
    • Training
  • Resources
    • Webinars
    • Blog
    • News
  • Contact Us

Global Clinical Affairs

  • Clinical Support (Drugs, Biologics, Medical Devices/IVDs & Combination Products)
  • Clinical Trial Strategy
  • Clinical Development Plans 
  • Clinical Trial Protocol Design & Development
  • Analyze & Interpret Clinical Trial Data 
  • Investigator Brochure Development
  • Safety Assessments, Periodic Safety Update Reports (PSURs), Benefit/Risk Assessments
  • Statistical Considerations, Analysis Planning & Reporting
  • Clinical Study Reports
  • EU MDR Clinical Study Plans & Reports
  • EU MDR General Safety & Performance Requirements (GSPR)
  • Medical Writing (Regulatory, Proposals, Grants, Narratives, White Papers, Journal Publications)

  • Home
  • Team of Experts
  • Operations Team
  • Areas of Expertise
  • Webinars
  • Blog
  • Contact Us

The Eriah Group, Inc.

Cleveland, Ohio

(440) 479-0511

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