HUD revises noise abatement regulations to allow multiple program offices to approve projects in unacceptable noise zones based on funding source and eliminates outdated surveillance requirements.
Total Nutrition Inc. expands recall of TNVitamins and Doctor's Pride Ultra Potent Complete Green Superfood Moringa Capsules due to potential Salmonella contamination identified during supply chain review.
FDA classifies Spinal Muscular Atrophy newborn screening test systems as Class II devices, requiring special controls to ensure safety and effectiveness while reducing regulatory burden for manufacturers.
FDA classifies simple point-of-care SARS-CoV-2 detection devices as Class II medical devices, requiring special controls to ensure safety and effectiveness while reducing regulatory burden for manufacturers.
FDA reopens the comment period for its industry guidance on scale-up and postapproval changes for drug dosage forms to allow additional stakeholder input.
FDA extends the comment period for its drug repurposing request for information to allow stakeholders additional time to submit input on addressing unmet medical needs.
Azuma Foods International recalls 545 cases of 3-pack Tako Wasabi seasoned octopus due to undeclared fish allergen that poses serious risk to consumers with fish allergies.
FDA seeks OMB approval for information collection requirements regarding establishment, maintenance, and availability of traceability records for certain foods under the Paperwork Reduction Act.
FDA submits proposed information collection procedures for safe processing and importing of fish and fishery products to OMB for Paperwork Reduction Act review.
HUD establishes a Privacy Act System of Records for Sumo Logic, a security monitoring tool that collects and aggregates system log data from HUD applications and infrastructure for centralized event correlation and analysis.
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