About us
Founded at the turn of the millennium, Replior began as provider of IT operation services for the Life Science industry.
Over the years, we’ve evolved, acquiring the Trial Online EDC software system in 2010 and setting out on a mission to become a trusted partner for data collection in clinical trials.
Our journey has been marked by collaboration, innovation, and a commitment to advancing patient care and research.
40+
Employees
23
Years in business
43
Languages supported on Trial Online Suite
30,154
Participants in the largest study run on our EDC System
Our Approach
We believe in the power of technology to transform clinical trials. But more than that, we believe in putting patients at the heart of everything we do. From introducing gamification elements to enhance patient engagement to developing the ePRO platform for streamlined and standardized data collection, we’re always looking for ways to make the clinical trial experience better for everyone involved.
Our Products
Our flagship offering, Trial Online, is a suite of systems designed to make data collection in clinical trials as seamless and efficient as possible. Whether it’s EDC, ePRO, eConsent, or Virtual Visits, we’ve got you covered. And with our capabilities to integrate with wearable sensors, we can provide robust measurements to provide evidence of your product’s efficacy.
Our Commitment
Honesty. Transparency. Integrity. These aren’t just words to us; they’re the principles that guide everything we do. We’re fully auditable, compliant with all relevant regulations, and dedicated to providing services that meet the highest standards of quality. Our IT operations boast certifications like ISO 27001, ISO 9001, ISO 14001, and PCI DSS, and our infrastructure is fully redundant, operating from geographically separated data centers.
Meet the team
Christer Nilsson
Jonas Billing
Steve Simpson
Jonas Boström
Anders Ottosson
Kikki Boström
Albana Shahini
Shaq Nejad
Åsa Gunnarsson
Maria Milas
Tony Forsberg
& Data Protection Officer
Therapeutic Areas
Trial Online has conducted 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 trial has never been easier.
- 100% Web-based EDC and ePRO
- Clients are able to perform all activities themselves
- Easy and fast set up of the complete system
- Fully compliant with 21 CFR part 11 and GCP
- Hosted on a secure dedicated server
- User-friendly
- Medical coding: MedDRA and WHO-DD
- Flexible and fast eCRF design
- Facilitates networking with specialists and partners
- Cost-effective even for small MedTech and BioTech studies
- Easy construction of Data Sets – adaptable data export
- E-training