Streamline your trial start-up with , the digital solution that simplifies patient onboarding with secure enrollment. Experience stronger engagement and full regulatory compliance for smoother clinical trials.
Provide on-demand support with integrated Q&A and multimedia tools accessible on any device, ensuring every patient is well informed.
Deliver eConsent content in every participant’s native language automatically for enhanced engagement and clear understanding.
Connect oomnia eConsent directly with your EDC and CTMS for perfectly aligned, efficient workflows.
Ensure audit-readiness and safeguard patient data with robust encryption and strict access controls.
Delight participants with an intuitive interface that simplifies consent and boosts engagement.
Enrich your consent process with interactive videos, Q&A sections, and vivid content that drives understanding.
Offer patients the choice of digital or paper consent, tailored to their needs for a truly adaptable experience.
Reduce costs and increase convenience with our web-based solution that works flawlessly on smartphones, tablets, and computers.
Generate custom graphical or tabular reports from any EDC data with role-based access, delivering actionable insights and audit-ready trails.
Create and export tailored data listings by selecting specific visits, pages, or fields to suit your study’s needs.
Inspired by the Latin Word omnia, Meaning 'All Things',
We Created oomnia.
A single, unified system that brings together every part of a clinical trial, from planning to global compliance.
EDC, RTSM, eTMF and CTMS, eSource, ePRO, eCOA and eConsent are integrative parts of one and the same ecosystem supporting multiple trials on a single instance.
Choose the modules and features that work for you and customize everything to fit your workflow.
Stay ahead with immediate notifications for incomplete processes or required actions, keeping your trial running smoothly and on schedule.
Meet global compliance with advanced digital signatures that support complex workflows, multi-signature processes, and complete traceability.
oomnia - Meeting Industry Standards
Our unified clinical trial software is designed with compliance at its core, meeting critical industry standards. Our commitment to these regulations ensures that your clinical trials are not only efficient but also adhere to the highest levels of data integrity, privacy, and ethical conduct.
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Empower participants to choose digital or paper consent, boosting access
Accelerate consents from weeks to minutes with rapid, secure signatures
Use live Q&A and multimedia to offer instant, clear guidance
Use live Q&A and multimedia to offer instant, clear guidance
Enhance compliance with forms in multiple languages for clear understanding
Seamlessly sync participant data across systems, cutting manual tasks
Looking to explore more? Get our eConsent flyer for more details.
Read more about the importance of eConsent in patient-centric clinical trials.
Get the answers you need about oomnia eConsent
eConsent (Electronic Informed Consent) software digitizes the informed consent process in clinical trials, replacing paper consent forms with interactive digital documents. Wemedoo's oomnia eConsent streamlines patient onboarding with multimedia content, multi-language support, and secure electronic signatures.
eConsent improves enrollment by making the informed consent process more accessible and engaging for patients. Interactive multimedia content helps patients understand complex trial information, remote consent enables participation from home, and the streamlined digital process reduces drop-off rates during the onboarding phase.
Yes, electronic informed consent is legally valid and recognized by the FDA, EMA, and other regulatory authorities. oomnia eConsent complies with 21 CFR Part 11, ICH GCP, and EU Clinical Trials Regulation requirements, with complete audit trails and tamper-proof electronic signatures.
Yes, oomnia eConsent supports extensive multi-language options for global clinical trials. Consent documents can be presented in the patient's preferred language, ensuring proper understanding and compliance with local regulatory requirements across different countries.
oomnia eConsent is natively integrated with the EDC system, so consent status is automatically updated in the patient record. This eliminates manual tracking, ensures no data is collected before consent is obtained, and provides real-time visibility into enrollment progress across all sites.