Deliver High-Quality Data during Clinical Trials
Our suite of Trial Oversight tools enables sponsors to develop interpretations, draw conclusions, and take action based on high-quality data that they can be confident in
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FULLY INTEGRATED SOLUTIONS BUILT FOR OPTIMAL SITE PERFORMANCE
Study information. Documents. Tasks. Sites. Collaborations. The wide-ranging list of components that must be administered and maintained throughout the course of a clinical trial goes on forever. And the task of managing and controlling them all is monumental. With PortalMedica, you can seamlessly connect clinical study data and effectively link all the documents on a single platform.
Automation can improve productivity for several areas within an every phase clinic. Whether it is volunteer recruitment, real-time study data collection, sample tracking, data management or reporting, PortalMedica will handle all your study needs.
This browser-based, tablet-compatible system provides an advanced platform for automating your clinic operations, complies with FDA 21 CFR Part 11 and supports standards such as CDISC for easy export and data reporting.
PortalMedica capabilities include the following:
- Comprehensive integration with a wide range of bedside patient monitoring, telemetry and clinical devices for real-time direct data capture of vital signs, ECG, body measurements, as well as the ability to attach files such as ECG traces.
- Searchable volunteer database for running recruitment campaigns with the ability to track interactions and maintain a status of current and past clinical trial participation.
- Ability to track samples through the clinic plus order and import lab results, enabling clinic staff to quickly and effectively respond to safety issues.
- Study team electronic notification alerts of research participant’s data or experiences, allowing them to take appropriate clinical action and medical intervention.
- Treatment blinding and allocation allows researchers to effectively track drugs per research participant for adherence to clinical plan and dosages, ensuring protocol compliance.
- Comprehensive array of data management capabilities, including time tolerances, soft and hard parameter ranges, calculations, traditional edit checks, query management, study locking and exporting data.
Services
Personalized Support
We adjust and support every document every time.
Training
Building great course materiales and training all the time.
AI & Big Data
Building insights to integrate and facilitate knowledge.
Team
Who We Are
Generate vertical integration while remembering to increase viewability. Grow social with the aim to increase viewability. Lead vertical integration in turn innovate.
Repurpose customer jounreys with the aim to come up with a bespoken solution. Growing benchmarking so that we build ROI.
Engage benchmarking to, consequently, take this offline. Execute user experience to go viral. Funneling sprints and possibly improve overall outcomes.