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Home » DOL-Labor Department

DOL-Labor Department

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  • Healthcare benchmark logo

    Benchmark: Pharmacy Benefit Manager Fee Disclosure Compliance for ERISA Group Health Plans

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    Pharmacy Benefit Manager Fee Disclosure Compliance for ERISA Group Health Plans

    $199.99
  • Healthcare benchmark logo

    Benchmark: Transparency in Coverage: Compliance and Data Reporting for Health Plans

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    Transparency in Coverage: Compliance and Data Reporting for Health Plans

    $199.99
  • Healthcare benchmark logo

    Benchmark: Federal-State Unemployment Compensation (UC) Program: Data Disclosure Compliance

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    Federal-State Unemployment Compensation (UC) Program: Data Disclosure Compliance

    $129.99
  • Healthcare benchmark logo

    Benchmark: Federal Independent Dispute Resolution (IDR) Correcting Amendment: Compliance and Implementation

  • an icon representing Public Health

    Federal Independent Dispute Resolution (IDR) Correcting Amendment: Compliance and Implementation

    $129.99
  • Construction and Urban-Development benchmark logo

    Benchmark: Rescission of Executive Order 11246: Federal Contracting Compliance Requirements

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  • Library
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  • Publication Year
    • 2024
    • 2025
    • 2026
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DOL-Labor Department

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FDA Class II Requirements for Wearable Vibration Orthopedic Devices

Nov 5, 2026

Why This Course is Important
Without this training, you risk overlooking critical compliance steps for FDA-approved wearable vibration orthopedic devices, which may lead to costly delays, regulatory penalties, and limited market access.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Medical Devices; Orthopedic Devices; Classification of the Wearable Vibration Device for Orthopedic Use.

Key regulatory references include:

  • 21 CFR Part 888 – Orthopedic Devices

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FR-26-3306-1

FDA Rule: Class II Classification of Prognostic Assessment Software for Mild Cognitive Impairment

Nov 5, 2026

Why This Course is Important
Without this course, you risk costly regulatory missteps, delayed market entry, and potential enforcement actions that could threaten the success of your prognostic assessment software for mild cognitive impairment.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Medical Devices; Neurological Devices; Classification of the Prognostic Assessment Software of Mild Cognitive Impairment.

Key regulatory references include:

  • 21 CFR Part 882 – Neurological Devices

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FR-26-3305-1

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