Clinical Trial Software Services

Clinical Trial Software Services

Replior’s Clinical Trial Software Services is operated through Trial Online

Trial Online EDC has been in operation since the beginning of 2000, as a trusted eCRF provider for thousands of clinical studies made over the years, from small Phase I trials to global Phase III/IV trials.

Trial Online ePRO provides Patient diary and questionnaire service to clinical studies.


Trial Online is a designed, developed, and tested computer system as defined in PIC/S ‘Good Practices for Computerised Systems In Regulated “GxP” Environments’. And Trial online is of course compliant with FDA 21 CFR Part 11.

Our Quality Management System is built on quality standards in the industry, e.g. guidelines and directives provided by ISPE, FDA and EMA.

Replior and Trial Online are audited regularly by its clients (regulated companies).

Trial Online EDC and Trial Online ePRO is owned, developed and qualified by Replior AB.



Virtual Visits

Trial Online EDC

Fast and easy data collection

All Trial Online activities are managed online and offer a modern and easily accessible platform for all involved in a study.

No special hardware or software is required to run the service, which utilizes standard internet browsers. Fast and easy set up no matter the size of the trial.

Trial Online ePro

Better data faster

Trial Online ePro lets you run the trial you want, and not the trial your system allows you to.

Assign defined user roles for an easier management, and automatic notify user about specific events. Divide questionnaires into time and date defined events, and get better insights faster.


Shift from paper-based to an online solution.

Paper free informed consent will not only improve quality and compliance but retention for your clinical trial.

eConsent provides patients with clear and understandable clinical trial information so you can make sure that they are fully informed before entering a trial.


Trial Online ePro Subject App

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