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Home » HHS:Food and Drug Administration » Page 11

HHS:Food and Drug Administration

Showing 91–99 of 189 resultsSorted by latest

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    FDA’s Proposed Reclassification of ISH Test Systems

    $49.99
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    FDA Classification for Inherited DNA Test

    $9.99
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    FDA’s Classification of Plazomicin Test System: Ensuring Safety and Innovation

    $9.99
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    FDA Requirements for Electrical Tongue Nerve Stimulators to Treat Motor Deficits

    $19.99
  • Healthcare benchmark logo

    Benchmark: FDA Proposed Reclassification of Oncology Nucleic Acid-Based Test Systems

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    Medical Device QMSR Technical Amendments: Editorial Updates for FDA Compliance

    $49.99
  • Benchmark: FDA Compliance Training: New Prior Notice Requirements for Imported Food by International Mail

    Benchmark: FDA Compliance Training: New Prior Notice Requirements for Imported Food by International Mail

  • Healthcare benchmark logo

    Benchmark: FDA Reclassification of Hepatitis B Virus (HBV) Assay Devices: Compliance and Implementation Training

  • Benchmark: FDA Regulatory Changes: Vitamin D3 Fortification in Yogurt and Cultured Dairy Products

    Benchmark: FDA Regulatory Changes: Vitamin D3 Fortification in Yogurt and Cultured Dairy Products

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    • 2024
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HHS:Food and Drug Administration

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FDA Compliance for Infant Pulse Rate and Oxygen Saturation Monitors (OTC)

Oct 10, 2026

Why This Course is Important
Without this course, manufacturers and sponsors risk missing vital regulatory updates, leading to potential denial of market access, costly recalls, or enforcement actions for non-compliance with FDA requirements.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Medical Devices; Cardiovascular Devices; Classification of the Infant Pulse Rate and Oxygen Saturation Monitor for Over-the-Counter Use.

Key regulatory references include:

  • 21 CFR Part 870 – Cardiovascular Devices

Course SKU
FR-26-3260-1

FDA Regulatory Requirements for Home-Collected STI Nucleic Acid Detection Systems

Oct 10, 2026

Why This Course is Important
Without this course, you risk missing critical updates to FDA requirements for STI diagnostic systems, potentially exposing your organization to recalls, import detentions, or lost market access due to non-compliance.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Medical Devices; Immunology and Microbiology Devices; Classification of the System for Detection of Nucleic Acid From Non-Viral Microorganism(s) Causing Sexually Transmitted Infections Using Home-Collected Specimens.

Key regulatory references include:

  • 21 CFR Part 866 – Immunology and Microbiology Devices

Course SKU
FR-26-3259-1

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