oomnia eConsent - 2026 Pricing, Features, Reviews & Alternatives

oomnia eConsent is a comprehensive digital solution designed to streamline the patient consent process in clinical trials. The system simplifies enrollment procedures while enhancing participant engagement and ensuring full regulatory compliance. The platform offers instant patient assistance through integrated question-and-answer functionality and multimedia tools that are accessible on various devices, ensuring participants remain well-informed throughout the consent process. The software supports multiple languages, automatically delivering content in each participant's native language to facilitate clear understanding and improved engagement.

The oomnia eConsent system integrates seamlessly with Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS), creating efficient workflows and reducing manual data entry. The platform prioritizes data security and compliance, implementing strict access controls and robust encryption to safeguard patient information while maintaining audit-readiness. Users benefit from an intuitive interface that simplifies the consent process and increases participant engagement through interactive videos, dynamic content, and comprehensive question-and-answer sections. The system accommodates both digital and paper consent options, allowing flexibility based on individual participant preferences and needs.

The platform features advanced capabilities including real-time action alerts that notify users of incomplete processes, next-generation digital signatures that support complex workflows with complete traceability, and dynamic reporting tools that generate custom graphical or tabular reports from EDC data. The system adheres to critical industry standards including 21 CFR Part 11, HIPAA, GDPR, ICH GCP, Swiss Data Privacy Law, and FAIR ALCOA principles.