Documents/FDA/5: More Effective Regulation Through a Stronger Workforce/5.4: IT

5.4: IT

Transition Information technology from an enabler to a strategic tool for realizing the FDA's policy goals and objectives.

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Currently, the FDA views information technology (IT) resources as a means for the agency's medical review staff to accomplish their day-to-day work. Information technologies help staff manage the volumes of information that the agency receives more efficiently, by minimizing storage and administrative overhead, for example. In the future, the FDA is going to view IT as a strategic tool that can be used by program staff to accomplish their policy goals and objectives with greater efficiency and effectiveness. One key action item for the FDA is the development of an integrated IT process for determining and managing Center-unique systems, FDA-wide systems, and HHS-wide systems. The FDA's blueprint calls for an IT capability that contributes directly to mission-critical goals, such as faster review of new drugs and medical devices, more rapid targeting of suspect imports, and quicker identification, analysis, and communication of medical errors and suspected problems with the use of new medical technologies.

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