Stay ahead with a course focused on the FDA’s new regulations for over-the-counter devices assessing sleep apnea risk. Learn which special controls and general requirements now apply, how to prepare your product for regulatory review, and what documentation and testing are necessary. Equip your team with actionable steps for software, labeling, and hardware compliance to avoid costly enforcement actions and ensure continued market access.
In this course you will learn the following:
* Understand the scope and intent of the FDA’s classification of OTC sleep apnea risk assessment devices.
* Identify and interpret the special controls and general controls applicable to these devices.
* Implement the required testing, labeling, and documentation to ensure compliance.
* Recognize the legal and regulatory consequences of failing to comply with the final rule.
