Modernize your informed consent process with Trial Online’s eConsent.


Tools to easily keep track of consent versions and participant approval to remain compliant. 

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eConsent Process Flow

Participant safety and integrity starts with the participant’s understanding of the trial and all of the inherent risks involved. This is where eConsent can offer more protection through a directed online experience. The step-by-step process guides the participant to ensure understanding and presents a signature box only at the end of these exercises.

Computer showing eConsent

Features:

Maximize Participant Retention

Paper-free informed consent will not only improve quality and compliance but retention for your clinical trial. eConsent provides participants with clear and understandable clinical trial information so you can make sure that they are fully informed when making a decision to participate in your trial. This saves not only time, which is critical for optimal launch timeframes, but money for your budget.

Create Cost Savings

Sponsors can achieve tremendous time and cost savings using eConsent by eliminating the costs involved in chasing, managing, and storing a paper trail. This further reduces the research team’s time involved in the consent process.

Real-time Data

eConsent provides real-time tracking of recruitment rates to trial sponsors. This is very important to get a consolidated view of trial progress and also to not risk going over set enrollment goals.

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ePRO

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Next-generation participant data collection for validated questionnaires on participants own phone, or Replior provided pre-installed phones.

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EDC

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Proven EDC system based on 20 years and over 1000 trials track record. Fully role-based to enable review, query, verify, approve and sign-off on forms to produce quality data.

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Virtual Visits

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Enable participant convenience of in-home virtual trial visits through video calls. Move visits from in-clinic to the home, conduct Virtual Visits to capture data, increase engagement and security.

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