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Home » DOT:Federal Aviation Administration » Page 11

DOT:Federal Aviation Administration

Showing 91–99 of 116 resultsSorted by latest

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    Enhancements to Eastern U.S. RNAV Routes: A Safety and Efficiency Course

    $9.99
  • icon showing a bride and railway

    FAA Directive Compliance for Rolls-Royce Trent XWB-97 Engines

    $19.99
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    Airworthiness Directives for Boeing 757 Structural Safety

    $9.99
  • icon showing a bride and railway

    FAA’s Proposed Update to Embraer Airworthiness Directives

    $9.99
  • icon showing a bride and railway

    Airworthiness Directives: Ensuring Safety in GE Engines

    $9.99
  • icon showing a bride and railway

    Master FAA Compliance: Airworthiness Directive 2024-26-02

    $9.99
  • icon showing a bride and railway

    Ensuring Compliance with FAA Directive on Airbus Nose Landing Gear

    $19.99
  • icon showing a bride and railway

    FAA Airworthiness Directives for Airbus SAS: Compliance Essentials

    $19.99
  • icon showing a bride and railway

    FAA’s Airworthiness Directive Compliance for Boeing 767

    $9.99
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  • Library
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  • Publication Year
    • 2024
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    • 2026
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DOT:Federal Aviation 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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