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FDA Rule: Anti-Phospholipase A2 Receptor Immunological Test System Classification & Compliance

$19.99

Stay ahead in diagnostics with this course tailored for manufacturers, laboratories, and regulatory professionals. Discover the FDA’s class II classification and special controls for anti-phospholipase A2 receptor immunological test systems. Learn precisely what design, validation, labeling, and documentation standards must be met for compliance, and the real-world consequences of missing the mark. This training demystifies the De Novo pathway and clarifies the steps required to market innovative immunology devices while maintaining FDA standards.

In this course you will learn the following:
* Understand the FDA’s classification process for new medical devices, specifically the De Novo pathway.
* Identify the key requirements and special controls for the anti-phospholipase A2 receptor immunological test system.
* Implement the necessary steps to ensure compliance with the new classification and labeling requirements.
* Recognize the legal and regulatory consequences of failing to comply with the final rule.

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 regulatory missteps, increased costs from delayed market entry, potential device reclassification, and even enforcement actions that could halt your ability to provide or use this diagnostic test.

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 Anti-Phospholipase A2 Receptor Immunological Test System.

Key regulatory references include:

Course SKU
FR-25-1482-1