The COVID-19 Vaccine Registry is a secure repository of data containing vaccine administration, utilization, and adverse event information for analysis by the research community. The weekly updated registry is not only critical for new COVID-19 vaccine-related research projects but also necessary in...
Friday, April 30, 2021 | 1:00-2:00pm | Via Zoom The Partners Biobank Portal is a tool that links consented subjects from the Partners 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...
Friday, April 30 | 10:00-11:00am | Via Zoom REDCap Representatives: Lynn Simpson, Research Data Collection Services Manager, Jeremy Alphonse, Research Data Collection Services Project Analyst, Research Information Science and Computing (RISC) Applications and Services Mass General Brigham (MGB) has...
Thursday, April 29 | 11:00am-12:30pm | Via Zoom 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...
Software SAS Licensing Available for Researchers & New Renewal Process The cost for SAS software remains at $300 per license annually, payable by fund number or cost center. Licenses will automatically renew on April 1st. To purchase a new license, please visit the ERIS Research Computing Core...
We proudly present RISC Dashboard: Research Information Science and Computing hosted by Collibra. The new data catalog tool is becoming a central location for the data definitions for assets within RISC repositories, starting with COVID-19 research tools and the RPDR data dictionaries. Any Mass...
Introduction to the Biobank Portal Friday, March 26, 2021 | 1:00-2:00pm | Via Zoom The Partners Biobank Portal is a tool that links consented subjects from the Partners Biobank with their health care data from the electronic medical record (EMR) and allows researchers to request clinical samples for...
Monthly REDCap User Group Meeting Friday, March 26 | 10:00-11:00am | Via Zoom REDCap Representatives: Lynn Simpson, Research Data Collection Services Manager, Jeremy Alphonse, Research Data Collection Services Project Analyst, Research Information Science and Computing (RISC) Applications and...
Introduction to the RPDR Thursday, March 25 | 11:00am-12:30pm | Via Zoom 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...
The Partners Biobank Portal is a tool that links consented subjects from the Partners 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...