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Introduction to the Research Patient Data Registry (RPDR)

Zoom (click website to register/receive link)

The Research Patient Data Registry (RPDR) brings clinical information to the researcher's fingertips and ensures the security of patient information by controlling and auditing the distribution of patient data within the guidelines of the IRB. This course will provide an introduction to the use of the RPDR (Research Patient Data Registry) application for clinical research, […]

REDCap: Survey Features & Functionality

Zoom (click website to register/receive link)

Learn how to create, send, and collect research data using the REDCap Survey feature. REDCap surveys provide a powerful tool for collecting responses from survey participants by 1) emailing or texting a link to your survey, 2) entering data direct on a tablet/kiosk, and/or 3) posting a links on websites. We will also review Responsy, […]

Biobank Portal Training

Zoom (click website to register/receive link)

The MGB Biobank Portal is a tool that links consented subjects from the MGB Biobank with their health care data from the electronic medical record (EMR) and allows researchers to request clinical samples for these subjects. This course will provide an introduction to the use of the Biobank Portal application for clinical research, including the […]

Introduction to the Research Patient Data Registry (RPDR)

Zoom (click website to register/receive link)

The Research Patient Data Registry (RPDR) brings clinical information to the researcher's fingertips and ensures the security of patient information by controlling and auditing the distribution of patient data within the guidelines of the IRB. This course will provide an introduction to the use of the RPDR (Research Patient Data Registry) application for clinical research, […]

REDCap: Getting Started

Zoom (click website to register/receive link)

Summary: In collaboration with the Harvard Catalyst, REDCap is a free, secure, web-based application hosted by MGB Research Computing and designed to support electronic data capture for research studies. To learn more about REDCap visit: http://rc.partners.org/edcredcap. This course will provide a high level overview of the REDCap tool. Learn about study start up, project life cycles, data […]

Biobank Portal Training

Zoom (click website to register/receive link)

The MGB Biobank Portal is a tool that links consented subjects from the MGB Biobank with their health care data from the electronic medical record (EMR) and allows researchers to request clinical samples for these subjects. This course will provide an introduction to the use of the Biobank Portal application for clinical research, including the […]

Introduction to the Research Patient Data Registry (RPDR)

Zoom (click website to register/receive link)

The Research Patient Data Registry (RPDR) brings clinical information to the researcher's fingertips and ensures the security of patient information by controlling and auditing the distribution of patient data within the guidelines of the IRB. This course will provide an introduction to the use of the RPDR (Research Patient Data Registry) application for clinical research, […]

REDCap: eConsent Functionality

Zoom (click website to register/receive link)

Mass General Brigham (MGB) has developed a REDCap eConsent Framework that will turn the paper-based informed consenting processes into an electronic informed consent process that researchers can use for Institutional Review Board (IRB) reviewed and approved studies. The MGB REDCap eConsent Framework will allow users to implement a combination of the validated components to design […]

Biobank Portal Training

Zoom (click website to register/receive link)

The MGB Biobank Portal is a tool that links consented subjects from the MGB Biobank with their health care data from the electronic medical record (EMR) and allows researchers to request clinical samples for these subjects. This course will provide an introduction to the use of the Biobank Portal application for clinical research, including the […]

Introduction to the Research Patient Data Registry (RPDR)

Zoom (click website to register/receive link)

The Research Patient Data Registry (RPDR) brings clinical information to the researcher's fingertips and ensures the security of patient information by controlling and auditing the distribution of patient data within the guidelines of the IRB. This course will provide an introduction to the use of the RPDR (Research Patient Data Registry) application for clinical research, […]

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