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FDA Regulation: Class II Classification of Menopause Test Systems

$19.99

Stay ahead with the latest FDA rule on menopause test systems. This comprehensive course covers the classification of menopause test systems as class II medical devices, highlighting the practical steps manufacturers and sponsors must take to comply with new special controls. Learn to meet rigorous design, validation, labeling, and documentation requirements to protect patient safety and maintain access to the U.S. market.

In this course you will learn the following:
* Understand the new classification and regulatory requirements for menopause test systems.
* Identify the special controls and general controls applicable to these devices.
* Implement the necessary steps to ensure compliance with the final rule.
* Recognize the legal and regulatory consequences of failing to comply with the classification and special controls.

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, you risk missing critical compliance steps, potentially facing denied market access, regulatory penalties, or legal action due to non-conformance with FDA requirements.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Menopause Test System.

Key regulatory references include:

Course SKU
FR-25-1489-1