Loss of patient data and prescription errors are just two potential safety risks associated with health IT (HIT) adoption. As the FDA examines these issues, the agency is questioning how to better regulate this new electronic field and which branch of government oversight is best suited to monitor such safety concerns.
In a letter to FDA Commissioner Margaret A. Hamburg, Senator Chuck Grassley (R-Iowa) asked for an update on the implementation of new guidelines for medical device makers on when they need to file new information with the agency and seek clearance for the marketing and use of modified devices under the 510(k) system.
Sen. Chuck Grassley, R-Iowa, has sent letters to 31 U.S. hospitals asking about their experiences in implementing health IT under the $19 billion American Recovery and Reinvestment Act of 2009 (ARRA). He is seeking to ensure the “effective and efficient use of taxpayer money” in implementing health IT, such as computerized provider order entry systems and EHRs.
The Senate Finance Committee voted today in favor of its version of proposed healthcare reform legislation in a 14-9 vote, including the approval of Olympia Snowe, R.-Me.
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