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IRT Support for a Long-Term, Complex Rare Disease Study

By Stephanie Kolp | July 31, 2025

Everest deployed its in-house IRT/RTSM technology, in addition to its expert team, to help the sponsor overcome several supply and dosing management challenges during a global, open-label extension study.

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16,000-Patient, Global Respiratory Trial that was Findings Free

By Stephanie Kolp | July 5, 2025

Everest provided biometrics and IWRS support to a large-scale, global Phase III trial spanning 26 countries. The FDA and EMA Inspection Reports had 0 inspection findings on the work performed by Everest.

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  • Everest Clinical Research Named Finalist of Fierce Outsourcing Awards for Excellence in Client Partnership
  • Who Should Own Your Clinical Study URL? A Practical Guide for Sponsors

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  • Services
    • Project Management and Clinical Operations
    • RBQM and Central Monitoring
    • Medical Monitoring
    • Pharmacovigilance
    • Data Management
    • Stats & Programming
    • DMC/DSMB
    • FSP Delivery Model
    • IRT/RTSM
    • ePRO/eCOA
    • Clinical Data Visualization
    • Regulatory Strategy
    • Regulatory Submissions
    • Medical Writing
  • Therapeutic Expertise
    • Therapeutic Areas
    • Case Studies
  • Quality
  • Careers
  • About Us
    • Company Overview
    • Leadership
    • Locations
    • News
  • Contact Us