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Medrio

Name: Medrio
Rating: 4.5 (2 reviews)

By Medrio

Medrio is an electronic data capture (EDC) tool for clinical research teams with tools for capturing, storing, analyzing, and managing patient data during clinical trials. Medrio offers secure storage of patient data, automates regulatory compliance management, and allows users to build custom studies. The cloud-based tool consists of four modules; electronic data capture (EDC), eSource for streamlining data entry, eConsent for gathering patient consent, and ePRO for reporting on patient outcomes. Medrio can be beneficial for medical sponsors, CROs, Pharma businesses, diagnostics teams, animal health professionals, and and any other type of industry that carries out clinical trials. The EDC module within Medrio facilitates the capture and input of data during clinical trials, with tools for building a custom database, creating and editing studies, and carrying out data checks. Users are able to build custom studies using the drag and drop interface, and edits can be made to studies at any time, even after the study in underway. Data can be entered into the Medrio EDC system using a desktop, mobile device, or iPad using the iOS and Android apps. In order to ensure that data is entered accurately, edit checks and data queries are carried out automatically and skip logic can be setup to prompt specific data entry. Medrio eSource offers mobile and tablet apps for capturing data electronically online or offline, either in a clinic or in the field. Users can access a range of forms for capturing data on individual patients, and this data can be shared instantly with real-time data sync. Consent can be confirmed with the Medrio eConsent module which facilitates electronic signature capture and consent form management. Consent forms can be created by study administrators in order to capture the necessary information to meet regulatory compliance, and to provide the customer with study information including videos, infographics, and more. The capture of PRO data can be managed using the ePRO module which offers tools for automatic survey delivery to patients, automatic notifications, capture of Quality of Life (QoL) metrics, patient reported information recording, and more.

890 Interested

Highlights : About Medrio

Electronic signature capture

Third party integration

Data capture and transfer

About Medrio

Medrio is an electronic data capture (EDC) tool for clinical research teams with tools for capturing, storing, analyzing, and managing patient data during clinical trials. Medrio offers secure storage of patient data, automates regulatory compliance management, and allows users to build custom studies. The cloud-based tool consists of four modules; electronic data capture (EDC), eSource for streamlining data entry, eConsent for gathering patient consent, and ePRO for reporting on patient outcomes. Medrio can be beneficial for medical sponsors, CROs, Pharma businesses, diagnostics teams, animal health professionals, and and any other type of industry that carries out clinical trials. The EDC module within Medrio facilitates the capture and input of data during clinical trials, with tools for building a custom database, creating and editing studies, and carrying out data checks. Users are able to build custom studies using the drag and drop interface, and edits can be made to studies at any time, even after the study in underway. Data can be entered into the Medrio EDC system using a desktop, mobile device, or iPad using the iOS and Android apps. In order to ensure that data is entered accurately, edit checks and data queries are carried out automatically and skip logic can be setup to prompt specific data entry. Medrio eSource offers mobile and tablet apps for capturing data electronically online or offline, either in a clinic or in the field. Users can access a range of forms for capturing data on individual patients, and this data can be shared instantly with real-time data sync. Consent can be confirmed with the Medrio eConsent module which facilitates electronic signature capture and consent form management. Consent forms can be created by study administrators in order to capture the necessary information to meet regulatory compliance, and to provide the customer with study information including videos, infographics, and more. The capture of PRO data can be managed using the ePRO module which offers tools for automatic survey delivery to patients, automatic notifications, capture of Quality of Life (QoL) metrics, patient reported information recording, and more.

Specifications

24/7 Support

Yes

Business Size

Mid-Market

Deployments

Cloud

Language Support

English

Platforms

Product Details

Features

Patient data collection

Electronic data capture (EDC)

Patient recorded outcomes

Double data entry

21 CFR Part 11 Compliance

Real time monitoring

Real time data

Real time notifications

Real time reporting

Third party integration

Drag & drop interface

Event triggered email

Electronic signature capture

Data entry verification

Data capture and transfer

Benefits

Collect data either in-clinic or on-the-go using any desktop, Android device, or iPad, and create custom workflows for data collection.

Use the drag and drop interface to build studies, adapted to clinic needs, without the need for programming knowledge, and make fast changes to studies whilst they’re underway.

Ensure regulatory compliance is always maintained throughout studies with Medrio’s automatic management of global data compliance regulations.

Confirm consent using the electronic signature capture tool, and create entire consent processes and forms with additional information provided via videos and graphics to ensure patient comprehension.

Ensure data entry is accurate with form rules including edit checks, skip logic, and data queries, to identify and data entry errors such as duplicates or missing fields.

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