openFDA
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Amazon hires openFDA trailblazer Kass-Hout for healthcare project: report
Amazon has hired former FDA chief health informatics officer Taha Kass-Hout, M.D., CNBC reports. Kass-Hout led the groundbreaking openFDA initiative and rehabilitated the reputation of the FDA’s IT department during his three years at the agency. Details of what Kass-Hout will do at Amazon are scarce....during his time at the FDA, Kass-Hout lead the precisionFDA program that established a collaborative, open approach to genomic testing references. Across the initiatives, Kass-Hout deployed approaches that were established in tech circles but alien to the FDA prior to his arrival. Open-source projects that embraced the cloud, shared their code on GitHub and invited programmers to hackathons became commonplace.
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API Provides Open Access To FDA Recall Data
As part of the Food and Drug Administration’s recently launched openFDA initiative, the regulatory agency is for the first time offering an application programming interface providing web developers and researchers direct access to millions of reports on drug adverse events and medication errors that have been submitted to the FDA since 2004...
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Dangerous Drug Attorney Jeffrey D. DeCarlo Comments On ‘OpenFDA’ Website’s Benefit To Consumers
Attorney Jeffrey D. DeCarlo, P.A. weighs in on the launch of the openFDA website, allowing consumers easier access to label information, recalls and other information about defective drugs and medical devices...
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FDA Embracing Cloud, APIs In OpenFDA Initiative
The U.S. Food and Drug Administration is leveraging the cloud as part of its openFDA initiative to make data on recalls and adverse events easily accessible to software developers and researchers...
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FDA Hits Tight Timeline for Start of precisionFDA Open Beta
FDA has hit the tight timeline it set itself for the start of the precisionFDA open beta program. The system went live this week, just as the regulator forecast when it started a closed beta program last month. Taha Kass-Hout, chief health informatics officer at FDA, committed to trying to have precisionFDA ready for testing by the end of the year back when the regulator first outlined the project in August. That Kass-Hout was willing to aim for such a timeline--which at the time he described as being "very, very tight"--and then went on to achieve it is testament to the new approach the regulator is taking to IT projects.
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FDA Releases Device Adverse Event API
Under its openFDA project, the U.S. Food and Drug Administration has released a new application programming interface that returns data from its Manufacturer and User Facility Device Experience (MAUDE), an FDA dataset that contains medical device adverse event reports...
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FDA Starts Beta-testing 'The Most Advanced Bioinformatics Platform in the World'
The FDA has started testing the precisionFDA platform it developed with DNAnexus. The closed beta test phase is the precursor to a more widespread rollout of the system, which the CEO of DNAnexus has described as being "the most advanced bioinformatics platform in the world." DNAnexus was enlisted by the FDA to help with the project in August...
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FDA’s Public Data Project To Get An Upgrade Under $1.2M Contract
In an ongoing effort to improve openFDA, San Francisco-based Iodine will work on making the portal more user friendly...
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Federal Open Source Is Messy - And That's OK
Open source projects like the National Library of Medicine's Pillbox show potential of open innovation -- including competition with projects started elsewhere...
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GSA’s Open Source First Approach Gives More Software Options, Better Savings
The General Services Administration last week announced a new policy requiring open source software be given priority consideration for all new IT projects developed by the agency. And while some may question whether open source software will be as effective as its conventional, proprietary counterpart, Sonny Hashmi, GSA’s chief information officer, is confident this new IT model will put the agency in the best position to procure and develop software in the most cost-effective manner. Read More »
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Health IT 2014: Interoperability, Ebola And Healthcare.gov 2.0
Health IT in 2014 continued its path toward a system of interoperable and open data to improve patient care with IT systems...
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How openFDA's 'Crazy Collision' of Silicon Valley and Federal Culture Is Reshaping the Regulator
Over the past two years the reputation of the IT department at the FDA has changed rapidly. Once best known for burning through CIOs and receiving slapdowns from the congressional watchdog, the FDA is now garnering plaudits for its embrace of agile and open development. This new way of thinking is central to--and to an extent responsible for--the recently unveiled precisionFDA initiative. Bio-IT World dug into the genesis of precisionFDA and its implications in a feature this week.
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OpenFDA Backstory: Breaking The Paperwork Backlog
The startup Captricity uses a combination of crowdsourcing and OCR to digitize mountains of paper records, particularly for government agencies and healthcare. Read More »
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openFDA Unveils Cache of Medical Device Data
OpenFDA is releasing information on medical devices that could spur innovation and advance scientific research. OpenFDA’s Application Programming Interface (API) expands the previous openFDA resources about medical device-related adverse events and recalls by incorporating information from the total medical device product life cycle. This includes current data on device classification (6000 records), 24,000 registrations of device companies and establishments, and the companies’ listings of over 100,000 devices. Data since 1976 on 30,000 device approvals and approval supplements, and 141,000 device clearance decisions (510(k) and de novo types) are now on openFDA.
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OpenFDA: Innovative Initiative Opens Door To Wealth Of FDA’s Publicly Available Data
OpenFDA is specifically designed to make it easier for developers, researchers, and the public to access and use the many large, important, health data sets collected by the agency.
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