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Suvoda eCOA

A better eCOA experience for patients, sites, and sponsors.

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Overview

Suvoda's eCOA is a key part of its eClinical platform that also includes IRT (Interactive Response Technology) and eConsent. The platform is designed to handle the complexities of modern clinical trials, such as oncology, CNS, and rare disease studies. By having eCOA, IRT, and eConsent on a single platform, Suvoda aims to streamline trial conduct, reduce site burden, and provide a more cohesive experience for patients. The solution supports BYOD and provisioned devices and is built to be intuitive for all users, from patients to study managers.

✨ Key Features

  • Single platform for IRT, eCOA, and eConsent
  • Designed for complex study designs (e.g., oncology, CNS)
  • Intuitive user interface for patients and sites
  • Supports BYOD and provisioned devices
  • Real-time data visibility and control
  • Agile study build process

🎯 Use Cases (4)

Complex therapeutic area trials (Oncology, CNS, Rare Disease) Patient-reported outcomes (PROs) Clinician-reported outcomes (ClinROs) Studies requiring seamless integration of patient reporting with randomization and trial supply

✅ Best For

  • Oncology trials with complex dosing schedules
  • CNS studies with frequent assessments
  • Rare disease trials with unique protocol requirements

💻 Platforms

Web iOS Android

✅ Offline Mode Available

🔌 Integrations

Suvoda IRT Suvoda eConsent EDC systems Drug supply management systems

🛟 Support Options

  • ✓ Email Support
  • ✓ Phone Support
  • ✓ Dedicated Support (Enterprise tier)

🔒 Compliance & Security

✓ SOC 2 ✓ HIPAA ✓ BAA Available ✓ GDPR ✓ ISO 27001 ✓ SSO ✓ ISO 27001 ✓ SOC 2 Type II ✓ GCP ✓ 21 CFR Part 11

💰 Pricing

Contact for pricing
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