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ICT eCRF & GDPR Compliance: Rules and Regulations

In May 2018, the new GDPR will came into effect, giving the already well-governed area of clinical trials even more regulations to comply with. The GDPR harmonised data protection regulations in the EU and replaced the current Data Protection Directive and national laws. The impact on clinical trials, sponsors, CROs and the software used needed executive attention and immediate action.
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Trial Online Product Overview

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Trial Online ePro Product Overview

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Trial Online Virtual Visits Overview

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Trial Online eConsent Overview

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Our Products

ePRO

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Next-generation patient data collection for validated questionaries on patients own phone, or Replior provided pre-installed phones.

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EDC

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Proven EDC system based on 20 years and over 1000 trials track record. Fully role-based to enable review, query, verify, approve and sign-off on forms to produce quality data.

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Virtual Visits

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Enable patient convenience of in-home virtual study visits through video calls. Move visits from in-clinic to the home, conduct Virtual Visits to capture data, increase engagement and security.

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eConsent

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Enables patients and researchers to take the first critical contact remotely in a safe and secure way

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