The Food and Drug Administration is extending until Feb. 5 the deadline for interested parties to submit comments and information to help the agency identify existing regulations and related paperwork requirements that could be modified, repealed, or replaced, consistent with U.S. law, to achieve meaningful burden reduction while allowing the FDA to achieve its public health mission and fulfill statutory obligations. Initially published on Sept. 8, the request for input involves the FDA’s general regulatory and information collection requirements as well as regulatory and information requirements by six product-oriented centers that carry out the agency’s mission.

ST&R: International Trade Law & Policy

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