OHDSI awarded $10 million FDA contract to support Biologics Effectiveness and Safety program

NewsGuard 100/100 Score

Researchers within the Observational Health Data Services and Informatics (OHDSI) community were recently awarded a $10 million contract from the U.S. Food and Drug Administration (FDA) to provide support to the Biologics Effectiveness and Safety (BEST) program, which was launched by the FDA Center for Biologics Evaluation and Research (CBER) in 2017.

The lead research team, primarily comprised of OHDSI personnel from Columbia University, UCLA, and Northeastern University, will provide support to the BEST system in its mission to conduct safety and effectiveness surveillance of biologic products (vaccines, blood and blood products, tissues and advanced therapeutics).

Specific means of FDA support through this grant will include serving in a convening role to develop methods related to using observational data from electronic health records and administrative claims to study the effectiveness and safety of biologics, work collaboratively with FDA staff to plan, develop, coordinate, host and convene meetings and workshops, and educate FDA staff and external stakeholders on the BEST infrastructure, capabilities, and applications that serve FDA and stakeholder needs.

We are very excited to partner with the FDA to address surveillance of biologics, including vaccine safety, as it brings the knowledge, experience, and tools of OHDSI to bear on problems critically important to the nation."

PI George Hripcsak, Chair and Vivian Beaumont Allen Professor of Biomedical Informatics at Columbia

"Sound approaches to monitor vaccine safety and effectiveness across large populations have their limitations; this is particularly important with the upcoming roll-out of COVID-19 vaccination programs, and we stand ready to help," said Marc Suchard, Professor of Biostatistics at UCLA, who will lead methods development under this contract.

"Northeastern is delighted to partner with Columbia and UCLA to support the FDA in this crucial endeavor," said David Madigan, Provost and Senior Vice President for Academic Affairs at Northeastern. "OHDSI supports a global community of researchers focused on generating reliable healthcare evidence. This project will greatly accelerate this work."

With collaborators from more than 30 nations around the world and over one billion patient records across 130 databases mapped to the Observational Medical Outcomes Partnership (OMOP) Common Data Model, the OHDSI community has both developed open-source tools to produce reliable, reproducible real-world evidence and published studies that have impacted both methodological research (LEGEND principles, ENCePP guidelines) and clinical decision-making (Lancet antihypertensive study, hydroxychloroquine safety profile).

Comments

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
Post a new comment
Post

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.

You might also like...
Research confirms no association between SARS-CoV-2 and childhood asthma diagnoses