$199.99
The newly revised Federal Management Regulation (FMR) is here—streamlining asset management, compliance, and operations across aviation, advisory committees, mail, motor vehicles, personal property, real property, and transportation. This course, built on GSA’s final rule and Executive Orders 14192 and 14219, details key statutory changes, compliance obligations, reporting requirements, and the broad economic and operational benefits for federal agencies. Gain actionable steps to implement the updated FMR and stay ahead of legal, financial, and operational risks.
In this course you will learn the following:
* Understand the scope and rationale for the FMR revisions.
* Identify and implement new compliance requirements across affected areas.
* Recognize the economic and operational impacts of the rule.
* Take actionable steps to ensure timely and effective compliance.
* Appreciate the consequences of non-compliance and the importance of regulatory streamlining.
NOTE: Unless otherwise indicated, all course purchases are for access to the course for a period of 1-year. At the end of the one year term, the course will be set to “inactive”.
Why This Course is Important
Without this course, learners risk missing critical statutory changes, failing to implement new compliance measures, and exposing their agencies to legal, financial, and operational penalties under the updated FMR.
Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Federal Management Regulation; Aligning the Federal Management Regulation (FMR) With the Administration’s Deregulatory Priorities.
Key regulatory references include:
Course SKU
FR-25-1637-1
CourseAvenue eLearning Platform has helped Federal agencies (and their suppliers) successfully address their most complex eLearning accessibility challenges.
Why This Course is Important
Without this course, you may overlook critical FDA requirements for HSV CNS diagnostic devices, risking compliance gaps and delayed market access.
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 Herpes Simplex Virus Nucleic Acid-Based Assay for Central Nervous System Infections.
Key regulatory references include:
Course SKU
FR-25-1407-1
Why This Course is Important
Without this course, professionals risk non-compliance with FDA device regulations, potentially delaying device approval, missing out on streamlined market access, and failing to implement critical safety measures that protect patients and support innovative diagnostics.
Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Medical Devices; Hematology and Pathology Devices; Classification of the Fluorescence In Situ Hybridization-Based Detection of Chromosomal Abnormalities From Patients With Hematologic Malignancies.
Key regulatory references include:
Course SKU
FR-25-1406-1
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