Enhancing speed and efficiency with oomnia eConsent
Effortlessly Obtain Participant Consent or Assent
- NSeamless eCRF and EDC integration
- NInteractive multimedia content
- NHybrid electronic and paper consent
- NWeb-based BYOD model
Enhancing speed and efficiency with oomnia eConsent
Effortlessly Obtain Participant Consent or Assent
- NSeamless eCRF and EDC integration
- NInteractive multimedia content
- NHybrid electronic and paper consent
- NWeb-based BYOD model
eConsent with oomnia
Patient-centric trials with oomnia eConsent
oomnia eConsent is purpose-built to be the most patient- and site-centric clinical trial management tool on the market. It can be used as a standalone software, however it truly comes to life as an essential component of our integrated clinical trial software, especially the EDC tools.
oomnia eConsent inherently enables patients to choose the most comfortable consent process. Both electronic and paper consent processes are simultaneously supported for all trials any time.
Our eConsent tool automatically presents informed consent documents in the participant’s chosen language, and a built-in Q&A module allows participants to directly communicate with site staff, fostering a supportive environment.
The digital process of oomnia eConsent cuts consent dissemination time from weeks to just a couple of minutes.
Experience a swift, secure, patient- and site-centric experience with our oomnia eConsent.
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.
Hybrid electronic and paper consent
Enhance accessibility with processes determined by the patient
Streamlined consent for sites
A revolution in the site facing consent process
Multilingual support
Enhance accessibility and compliance through language options
Interactive support features
Real-time communication to streamline participant interaction


Digital signatures
Accelerating the consent process with rapid digital signatures
Seamless platform integration
Flawless data synchronization for efficient trial management
Improved participant engagement
Fostering better interaction and compliance through convenient features
oomnia eConsent is designed to maximize participant engagement by making the consent process as straightforward and interactive as possible. The combination of multilingual support, real-time Q&A capabilities, and quick digital signing enhances participant satisfaction and retention. This proactive approach to participant interaction not only improves compliance but also contributes to more reliable and valid trial outcomes.
Access the eCONSENT Data Sheet
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Key features of oomnia
Streamlining clinical trials with unmatched efficiency and compliance
Seamless implementation
Compliance and security
Convenient user experience
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