Stay at the forefront of clinical laboratory regulation with this in-depth course on the CMS and CDC Request for Information regarding updates to the Clinical Laboratory Improvement Amendments of 1988 (CLIA). Learn how advanced testing technologies—from breath analysis to artificial intelligence—are shaping regulatory priorities. Understand the public comment process, key focus areas such as emergency preparedness, biosafety, and specialty testing, and discover how your feedback can influence future laboratory standards. Be prepared to contribute informed input that will impact laboratory operations and patient care nationwide.
In this course you will learn the following:
* Explain the purpose and intent of the RFI and the goals of potential CLIA regulatory updates.
* Identify the key topics and areas for which CMS and CDC are seeking public input.
* Describe the process and importance of submitting public comments.
* Recognize that the CLIA regulations are not being changed at this stage and may evolve based on stakeholder feedback.
* Summarize the main areas of inquiry and the types of information being solicited.
