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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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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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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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