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Home » HHS-Health and Human Services Department » Page 11

HHS-Health and Human Services Department

Showing 91–99 of 476 resultsSorted by latest

  • Healthcare benchmark logo

    Benchmark: CY 2027 Medicare Home Health Prospective Payment System Proposed Rule

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    CY 2027 Medicare Home Health Prospective Payment System Proposed Rule

    $199.99
  • an icon representing Public Health

    FDA Compliance for Skin Patch Devices Treating Hyperhidrosis

    $19.99
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    FDA Compliance Requirements for Opioid-Induced Oxygenation Monitors

    $19.99
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    FDA Classification and Compliance for Medial Knee Implanted Shock Absorbers

    $19.99
  • Benchmark: FDA Proposed Rule: Establishment Registration and Product Listing for Tobacco Products

    Benchmark: FDA Proposed Rule: Establishment Registration and Product Listing for Tobacco Products

  • FDA Proposed Rule: Establishment Registration and Product Listing for Tobacco Products

    FDA Proposed Rule: Establishment Registration and Product Listing for Tobacco Products

    $199.99
  • an icon representing Public Health

    Sponsor Assessment Updates in the Unaccompanied Children Program (Proposed Rule)

    $129.99
  • an icon representing Public Health

    FDA Requirements for Prognostic Test Classification: Preeclampsia Risk Assessment

    $9.99
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  • Publication Year
    • 2024
    • 2025
    • 2026
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HHS-Health and Human Services Department

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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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