The US Food and Drug Administration, without being named directly in a presidential memorandum, has been ordered to cease its attempts to secure pre-emptive regulatory authority over the 50 states on safety labeling, including for pharmaceuticals. In addition, the document calls for "heads of departments and agencies [to] review regulations issued within the past 10 years that contain statements in regulatory preambles or codified provisions intended by the department or agency to pre-empt state law, in order to decide whether such statements or provisions are justified under applicable legal principles governing pre-emption."
Peter Pitts, a former Associate Commissioner at the FDA and president of the Center for Medicine in the Public Interest, commented on former president of the Harvard Law Review, Pres Barack Obama's move: "this should put to bed any lingering doubts as to the Administration's views on the topic. 'Happy hour' for the trial bar [lawyers] begins immediately."
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