Project cooperationUpdated on 19 September 2023
We offer tailored services related to the conduct of Clinical Trial: Remote Trial Monitoring and Online Trial Management
About
What type of organisation are you looking for? (Question for consortium/coordinator seeking partners)
Mcr Clinic is looking for willing clinical sites that want to automate clinical trial management and Sponsors (pharmaceutical companies) that want to remotely monitor clinical trials. We allow a smooth transition into #HybridModel of Clinical Trials with a reduced number of physical (on-site) monitoring visits, remote access to eSource data, and remote monitoring of Clinical Trials without ‘over the shoulder’ access. This means reducing the number of physical visits by monitors to sites and, over time, abandoning traditional methods altogether in favor of remote trial monitoring and online trial management.
What kind of expertise are you looking for? (Question for consortium/coordinator seeking partners)
We develop the MCR Clinic system based on the great knowledge and experience of the originator, who has monitored clinical trials for many years. We are also assisted in software development by friendly researchers and monitors, so every feedback on our system is of great value to us.
What would you bring to a consortium? (Question for partner seeking consortium)
MCR Clinic™ helps Investigators and Site Teams with Trial Management (Online) as well as Monitors and Project Teams with Trial Monitoring (Remote) through: MCR Clinical Site Manager™ (CSM™) for Site Managers, Clinical Research Coordinators, Principal Investigators, Investigators and other Site Team members for effective contracting, startup, supervision and billing. MCR eSource Remote Viewer™ (eSRV™) for Monitor Coordinators, Monitors and other Project Team members for diligent full-scale remote monitoring on a day-by-day basis. MCR Clinic™ system ensures the security of anonymized patient data and blocks any unauthorized access. MCR Clinic™ strongly discontinues manual data entry and manual verification in favor of automated and secure workflow without fear of losing or risk of misconducting important source data. With MCR Clinic™ Investigators and Site Teams as well as Monitors and Project Teams may focus on medical issues and key challenges. MCR Clinic™ will do the rest integrating Clinical Trial with source EHR
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