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Replior is a privately held Swedish software solutions company focused on clinical trial support systems and offering a full suite of data collection products.
Replior develops in-house software and delivers Software as a Service, SaaS, solutions to Pharma companies and CROs.
The company is headquartered in Stockholm and has offices in Lund, Sweden, and Split, Croatia.
The EDC product Trial Online has been in operation since the year 2000, collecting data in over 1000 trials. Trial Online is 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.
About Trial Online EDC and ePRO
In early 2016, Trial Online ePRO was launched. Trial Online ePRO can be used as an integrated service with Trial Online EDC or as a stand-alone service.
In 2019, the Trial Online ePRO app and eConsent tool was launched.
Trial Online is owned by Replior AB as a part of the Hiberion Group.
See our policies:
Trial Online has conducted over 1000 studies in a wide range of therapeutic areas. Our software can accommodate the most complex of clinical trial designs, with an easy and time-saving set-up. Conducting a study has never been easier.
Trial Online is a designed, developed, and tested computer system as defined in PIC/S ‘Good Practices for Computerised Systems In Regulated “GxP” Environments’. Trial Online is, of course, compliant with FDA 21 CFR Part 11.
Our Quality Management System is built on quality standards in the industry, guidelines, and directives provided by ISPE, FDA, and EMA. Replior and Trial Online are audited regularly by its clients (regulated companies).
We are dedicated to delivering a service of the highest quality in all aspects of our operation. Continually striving to exceed customer expectations while consistently meeting their needs.
From development, through general product release, we have a high focus on quality and compliance. We have accomplished this by leveraging the latest technological solutions and regulatory standards such as:
All systems and processes used to manage a clinical trial are part of a regulated process that must be validated and needs to meet both FDA regulations and ICH guidelines. All Trial Online’s products follow these guidelines as well as industry standards to ensure product quality. This includes Software Development Life Cycle, System Qualification, and Quality Assurance Testing.
