Notice 24 Jul 2025 compliance, grants, national institutes of health, advisory council, health technology, human genome research

🧬Notice of Meeting for National Advisory Council on Human Genome Research

The Department of Health and Human Services announces a hybrid meeting of the National Advisory Council for Human Genome Research to discuss program relevance, including funding and regulatory matters. Open to the public, the meeting provides a platform for written comments, highlighting its significance for stakeholders in the health and research sectors.

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Rule 13 Jun 2025 regulatory compliance, fda, laboratories, medical devices, health technology, biologics, diagnostic tools

🦠FDA Classifies Fungal Nucleic Acid Detection Device to Class II

The Food and Drug Administration (FDA, Agency, or we) is classifying the device to detect and identify fungal nucleic acids directly in respiratory specimens into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the device to detect and identify fungal nucleic acids directly in respiratory specimens' classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.

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Rule 2 Jun 2025 radiation protection, fda regulations, medical devices, health technology, x-rays, radiology, classification

🩻FDA Classifies Radiological Devices to Enhance Market Access

The Food and Drug Administration (FDA, the Agency, or we) is classifying the radiological acquisition and/or optimization guidance system into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the radiological acquisition and/or optimization guidance system's classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices in part by reducing regulatory burdens.

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Grant Opportunities, Financial Assistance Programs, Professional Events 15 Jan 2025 grants, nih, research funding, health technology, federal meetings