Set up in hours.
Not weeks. Not months. Hours.
Clinical trials changed.
YOUR ePRO DIDN'T.
Patients live on their phones. Your ePRO still asks them to download an app. Create a password. Verify three times. We're building something different. A no-download, mobile-first ePRO designed for real life, not another system patients abandon.
This is still how trials run.
Slow, unresponsive screensTiny text that won't zoomComplex appsDevices no one knows how to useSlow, unresponsive screensTiny text that won't zoomComplex appsDevices no one knows how to useSlow, unresponsive screensTiny text that won't zoomComplex appsDevices no one knows how to useSlow, unresponsive screensTiny text that won't zoomComplex appsDevices no one knows how to use
Diary entries no one completesHigh dropoutMissing or unverified dataPasswords no one remembersDiary entries no one completesHigh dropoutMissing or unverified dataPasswords no one remembersDiary entries no one completesHigh dropoutMissing or unverified dataPasswords no one remembersDiary entries no one completesHigh dropoutMissing or unverified dataPasswords no one remembers
And paper? That's still happening too
Patients forget passwords. Sites reset them. Again. Entries come in late. Or not at all. Compliance follows up. Data gets patched. And everyone moves on.
Because "that's just how it is."
There is a different approach to ePRO: QClinical.
A no-download, mobile-first ePRO, designed for real-world patient behavior.
Patients receive a link. They complete it on their own phone. Data flows in real time. No devices to ship. No help desk calls. No missing entries.
Onboard in a minute.
No apps. No passwords. A link is all it takes.
Real-time data, instantly.
Real-time. Timestamped. Audit-ready.
QClinical isn't just a new ePRO.
It's what happens when you design for patients first.
QClinical is built around how patients really respond. In moments. On their phones. In between everything else.
Quick. Focused. Designed to be completed, not abandoned.
No long forms. No endless scrolling. No "I'll get back to it later."
Because that's what breaks ePRO. Not the questions. The experience.
And this isn't theory. It's already how modern medical content works. Qoolo's patent-pending micro-content engine powers how life sciences teams create, approve, and scale compliant content every day. QClinical brings that same thinking to clinical trials.
Micro-content changed how HCPs consume science.
Now it's changing how patients complete trials.
The answers you're looking for:
QClinical is a no-download, mobile-first ePRO experience for clinical trials, powered by the Qoolo platform. It's being built to help life sciences organizations create and deliver patient experiences for clinical studies without the apps, passwords, and multi-step verification that traditional ePRO tools rely on.
QClinical is being designed for pharmaceutical, biotech, MedTech, CRO, and clinical research teams responsible for patient engagement, patient-reported outcomes, and other digital study activities, from a single, no-code environment.
Traditional ePRO platforms were built primarily to collect patient-reported outcomes, and that remains essential to clinical research. But today's studies often need a broader digital experience that supports patients throughout their participation, not just at the moment data is collected.
QClinical is being built to expand what ePRO can do, aiming to help life sciences organizations create connected digital experiences, including study guidance, symptom diaries, reminders, and educational content, alongside patient-reported outcomes collection.
Yes. QClinical is being designed to remove common barriers to digital participation by letting patients access ePRO questionnaires and other study activities directly from their mobile device or web browser, without downloading an app or creating an account.
The plan is for patients to simply access the study using a secure link or QR code provided by the research team, making it easier to begin participating from their own mobile device.
QClinical is being designed with the requirements of regulated clinical research in mind. Audit trails, version control, and centralized content management are intended to help study teams maintain oversight of patient-facing content and document changes throughout a study.
By keeping study content and updates in one place, QClinical aims to support consistent processes and help organizations prepare for internal governance and audit requirements.
Yes. QClinical is not yet publicly available. We're currently preparing for launch and working with partners to refine the platform. If you're interested in learning more or exploring whether QClinical could support your clinical studies, we'd be happy to schedule a conversation and tell you more.