Center for Scientific Review will hold closed meetings to review research grant applications and provide advice on scientific matters to the National Institutes of Health.
Foreign-Trade Zone 78 in Columbia, Tennessee accepts notification of proposed production activity for polyethylene terephthalate preforms by Petainer Manufacturing USA, Inc.
Denial of Production Authority for Phillips 66 Company's renewable fuels and by-products facility in Foreign-Trade Zone 3 at Rodeo, California.
Final rule eliminates obsolete regulations governing repatriation and care of US nationals returned from foreign countries, streamlining bureaucratic requirements for human services and emergency response programs.
Center for Scientific Review amended notice of meeting for the National Institutes of Health scientific review group; meeting details and date available in Federal Register notice.
The Agency for Healthcare Research and Quality seeks OMB approval to extend the AHRQ Research Reporting System information collection with reduced annual burden and expanded scope to include grants, contracts, and challenge competitions.
USDA amends Title VI Civil Rights Act regulations to eliminate disparate-impact liability and align with Department of Justice standards under Executive Order 14281, reducing compliance costs for regulated entities.
FDA classifies ingestible gastrointestinal blood detection capsules as class II devices, establishing special controls to ensure safety and effectiveness while reducing regulatory burden for manufacturers.
FDA classifies radiological machine learning-based quantitative imaging software with predetermined change control plans as Class II medical devices, subject to special controls to ensure safety and effectiveness.
Foreign-Trade Zone 41 in Waukesha, Wisconsin proposes a dedicated computing activity for computer systems production with duty and tax deferral benefits for qualifying manufacturers.
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