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In the News: Data Driven Medicine – Informing the Cure

Getting a firm handle on what’s best for whom is a pressing quest of national healthcare reform — and Temple is working at its leading edge. Anuradha Paranjape, MD, MPH, FACP, Professor of Medicine and Chief of General Internal Medicine at Temple is lead investigator within a four-university consortium awarded a $7 million grant to … Continue reading In the News: Data Driven Medicine – Informing the Cure

PCORnet’s Richesson Elected Fellow of ACMI

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Rachel L. Richesson, PhD, with the PCORnet Rare Disease task force and the NIH Collaboratory Phenotype Core lead, has been elected a Fellow of the American College of Medical Informatics (ACMI), one of 19 people given this honor in 2014. ACMI is a college of elected Fellows from the U.S. and abroad who have made … Continue reading PCORnet’s Richesson Elected Fellow of ACMI

In the News: ClinicalTrials.gov: An Underutilized Source of Research Data

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Therapeutic Innovation and Regulatory Science, DIA ClinicalTrials.gov: An Underutilized Source of Research Data About the Design and Conduct of Commercial Clinical Trials Abstract Since 2007, the US federal government has required that organizations sponsoring clinical trials with a least one site in the United States submit information on these clinical trials to an existing database: … Continue reading In the News: ClinicalTrials.gov: An Underutilized Source of Research Data

NIH Notice: Revised definition of “Clinical Trial”

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The NIH has revised its definition of “clinical trial.” The revision is designed to make the distinction between clinical trials and clinical research studies clearer. It is not intended to expand the scope of the category of clinical trials. Notice of Revised NIH Definition of Clinical Trial (NOT-OD-15-015) National Institutes of Health

There’s a Giant Job Ahead for Big Data

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U.S. News & World Report, Kate Green, posted 10-3/14 Can analytics produce better outcomes? PCORI’s Joe Selby and Rachael Fleurence are featured in this article highlighting PCORnet as a leader in the movement to use electronic health records and other data sources to improve medical treatment. Read the full article …

Design Power: Patients Play Researchers in Drug Trials

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Scientists regularly sign up patients in clinical trials to test new treatments. Now, they are seeking patients to help them design some of those trials.

Patients and researchers can bring different perspectives to treating disease. In a trial of a potential prostate-cancer drug getting underway at the Icahn School of Medicine at Mount Sinai in New York, doctors had planned to ask patients periodically about side effects such as nausea. But patient input convinced them to ask additional questions, including how many days patients felt well enough to go to work.
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Free the Data announces new partnership with Rep. Debbie Wasserman Schultz

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WASHINGTON, DC. Posted: October 8, 2014, Free-the-Data.org Congresswoman continues her dedication to advancing medical research and improving care for hereditary breast and ovarian cancer Free the Data, a national coalition of organizations dedicated to freeing genetic information, today announced that U.S. Rep. Debbie Wasserman Schultz (FL-23) has been named its Honorary Chair. “The time for … Continue reading Free the Data announces new partnership with Rep. Debbie Wasserman Schultz

Mini-Sentinel Assessments

September 22, 2014 Mini-Sentinel is a pilot project sponsored by the U.S. Food and Drug Administration (FDA) to create an active surveillance system – the Sentinel System – to monitor the safety of FDA-regulated medical products. Most Mini-Sentinel activities focus on assessments, methods, or data. Visit the following links to learn more about each type … Continue reading Mini-Sentinel Assessments

FDA releases action plan to encourage greater patient diversification in trials

The FDA has released an action plan aimed at encouraging more diverse patient participation in drug and medical device clinical trials.

The plan, released last month, lays out priorities for increasing both trial participation and the reporting of patient demographic data. It follows an August 2013 report to Congress on these concerns.
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In the News: 5 Q’s for Sarah Greene, Senior Program Officer at PCORI

Published on September 2, 2014 | by Daniel Castro, Center for Data Innovation The Center for Data Innovation spoke with Sarah Greene, a senior program officer at the Patient-Centered Outcomes Research Institute (PCORI), a non-profit organization authorized by Congress to fund and disseminate research that will help patients and caregivers make more informed decisions. Greene … Continue reading In the News: 5 Q’s for Sarah Greene, Senior Program Officer at PCORI