This course provides a comprehensive overview of the FDA’s classification of pediatric continuous renal replacement therapy systems as class II devices with special controls. It focuses on safety, effectiveness, and compliance requirements crucial for manufacturers and healthcare providers. Gain insights into the regulatory framework that enhances patient access to innovative renal therapy devices.
In this course you will learn the following:
* Understand the classification process and criteria for the pediatric continuous renal replacement therapy system.
* Identify the special controls required for compliance.
* Recognize the potential risks and mitigation measures associated with the device.