FDA seeks public comment on a proposed Potential Tobacco Product Violations Reporting Form; 60-day comment period required under the Paperwork Reduction Act of 1995.
HHS updates its Temporary Assistance for Needy Families (TANF) Data system of records (System No. 09-80-0375) under Privacy Act requirements to include client data and verification information from state, territorial, and tribal TANF grantee agencie…
Center for Scientific Review holds closed meetings to review grant applications and provide confidential feedback to NIH-funded research institutions; specific dates and locations available through NIH official channels.
Center for Scientific Review holds closed meetings for grant peer review panels to evaluate National Institutes of Health funding applications.
FDA Form 3975 identity certification information collection has been submitted to OMB for Paperwork Reduction Act review under standard federal clearance procedures.
NIH Office of Laboratory Animal Welfare seeks 30-day public comment on a proposed chimpanzee research use data collection form before OMB review.
FDA classifies endoscopic light-projecting measuring devices as class II medical devices subject to special controls for gastroenterology-urology applications.
FDA classifies endoscopic traction devices as Class II medical devices, requiring special controls to ensure safety and effectiveness while reducing regulatory burdens for manufacturers.
FDA withdraws approval of Epizyme's TAZVERIK (tazemetostat) 200mg tablet following the company's voluntary request for NDA withdrawal.
HRSA corrects the 340B Rebate Model Pilot Program Information Collection Request to reflect 793,091 total estimated responses instead of 793,080, accounting for 11 manufacturer plan submissions.
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