✍🏾 eConsent
full transparency for you and your participants
🤝🏽 On web or smartphone
with full audit trails of signatories
Eligibility criteria
Write inclusion and exclusion criteria into your consent document so that you only enrol the right cohort for your research.
Participant information sheet (PIS)
Fill out your eConsent form with as much information as is appropriate for your study.
PDF copies
Digital eConsent copies are encrypted and backed up but are also shared with the participant and any study team members needed.
Version control
If you need to make any changes to a consent document, Trialflare's version control prevents participants from digitally signing expired consent forms.
Rich text and images
Dress-up your consent documents with any additional information you need - whether it's styling for converying critical information or useful imagery.

Trialflare has proved a really accessible way to collect data

"Being able to use a personal mobile means that staff who do not have access to a computer during their working day can be included in research and evaluation projects, and it avoids the time and expense of having to rely on pen and paper.”

Dr. Clare Wright
Consultant Clinical Psychologist and Systemic Psychotherapist, NHS Wales

[It was] easy for coordinators and participants to navigate and get involved with using iPads

"Data automatically synced as it was captured, allowing the research teams to directly access it without involving any extra work for our coordinators."

Dr. Maria Hristova
Project Leader, Comac Medical CRO

We are very pleased with the performance of this platform

Trialflare enabled us to complete anonymised cognitive tests at regular intervals and to record (paperlessly) details of lifestyle changes and wellbeing metrics over a period of nine months.Via the platform, these data were efficiently and accurately captured remotely with a low level of resource commitment.

Dr. Sue Plummer
CEO & Research Director, Cultech Ltd
⚖️ Comprehensively compliant
adherent to GDPR / HIPAA / MHRA / HRA / EMA guidelines and more
Anonymisation tools to help support anonymity of participants. Participants can also be auto-allocated to groups and pseudo-randomised where needed.
Hide personal information
Customise and store any personally identifiable information you need to whilst keeping it locked-down to study team members with the correct access privilages.
User lockout
If participants have not provided consent they cannot login. Trialflare's participant app prevents unwilling or uninformed participants from risking their safety.
Get the greatest confidence when enrolling participants with two-factor authentication. Unique one-time codes sent by SMS to help validate their identity.
Seriously secure
Everything in Trialflare is encrypted at rest and in transit and any links that are provided need authenticated users to access data. These links also expire after a short time.
🔐 Secure but accessible
and easy setup for users of all skill levels

🔗 URLs for sharing

Keep it as a URL for advertising yourstudy, or,transform it into a QR code for easy scanning with smartphone cameras.

Beautiful interface
Easy to navigate tabs with discrete functions that help you break apart bigger tasks into small manageable chunks.
Assign key users
Assign a consent champion or moderator to oversee all eConsent submissions.
Easy to make changes
If your IRB or REC require you to make changes, make any version changes you need to at the click of a button.
🤝🏽 All Trialflare solutions
learn more about all of other solutions here
Beautiful and responsive eCRFs with advaned functionality for users of all skill levels.
eCRF Solution
Gather data from participants from wherever they are and in multiple languages.
ePRO Solution
Protect your participants with full transparency and all the information they need to make a decision on whether to take part in your research.
eConsent Solution
Ensure participant identity protection with tools to auto-allocate IDs and treatment groups rich in powerful automations.
Randomization Solution