Study Portals
Secure study-specific web portals allow authorized members of a project team to communicate, learn and access study-specific documentation at any time and from anywhere around the globe, 24 hours a day/7 days a week. Access to each study portal is password protected, and information and access is assigned on a role-specific basis.
Study portals provide an operational dashboard and collaboration space; streamlining review processes and improving efficiency. Document tracking is automatic and all other information is mapped directly to project tracking and statistical tools to ensure accuracy. Study-specific web portals can be branded to each sponsor and offer advantages beyond traditional CTMS capabilities.
Training Portals
MedTrials is the ideal clinical trial management partner to clients who want reliable data from protected patients—done the right way, the first time—using established systems, efficient processes, and technology solutions to deliver results.
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Data management solutions should be customized to satisfy client, regulatory, and scientific needs. Through innovative data management solutions, MedTrials partners with you to ensure that your data is valid, reliable, complete, and accurately reported.
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Based on our extensive hands-on experience and industry wide leadership, MedTrials clinical research professionals offer in-depth and applicable training programs.
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As an approved Independent Review Organization (IRO), MedTrials can assist with compliance program planning and implementation to ensure you are always inspection ready.
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