Center for Scientific Review announces amended meeting notice with updated date, time, or location for stakeholder participation in peer-review policy discussions.
National Institute of Environmental Health Sciences holds a public meeting to discuss environmental health research priorities and grant funding opportunities for small businesses and academic institutions.
National Institutes of Health Director's office will hold a closed meeting to discuss pending grant applications and scientific review matters.
FDA proposes requiring foreign tobacco product establishment owners and operators to register with the agency and list their products, extending current domestic-only registration requirements to close information gaps.
CDC renews the charter for the Advisory Committee on Breast Cancer in Young Women to continue providing guidance on breast cancer prevention and treatment in younger populations.
HRSA's Rural Health Care Coordination Program submits revised performance measures (OMB No. 0906-0024) for OMB review; public comments accepted for 30 days before approval.
FDA's Cellular, Tissue, and Gene Therapies Advisory Committee will hold a public meeting to review Capricor's biologics license application for Deramiocel, a cell therapy product, with public comment accepted via docket submission.
Center for Scientific Review will hold closed National Institutes of Health peer review meetings to discuss grant applications and personnel matters on specified dates.
FDA determines the regulatory review period for VYALEV human drug product patent extension purposes and publishes this notice as required by law.
FDA classifies medial knee implanted shock absorbers as Class II devices subject to special controls to ensure safety and effectiveness while reducing regulatory burden for manufacturers.
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