MDRAO Practice Exam 2025 – Complete Exam Prep Resource

The requirement for an internal chemical indicator placed inside each package undergoing sterilization is based on the need to verify that the sterilization process has effectively penetrated the packaging and reached all sterilizable surfaces of the contained items. This is essential for ensuring that the items are indeed sterile and safe for use.

By placing an internal chemical indicator within each package, the healthcare facility can monitor the conditions of the sterilization cycle, such as temperature and pressure, and confirm that these conditions were met. The indicators change color when exposed to the appropriate sterilization parameters, providing a visual cue that serves as a safeguard in the quality assurance process of medical device reprocessing.

Without this internal indicator, it becomes challenging to validate that the entire content of the package has been adequately sterilized, increasing the risk of infection due to contaminated instruments. Hence, the requirement is a critical component of infection control standards in healthcare settings, making the statement factual.