Certified Professional in Health Care Risk Management (CPHRM) Practice Exam 2025 - Free CPHRM Practice Questions and Study Guide

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What is a key responsibility of the FDA?

To enforce insurance laws

To ensure the safety of medical devices

The key responsibility of the FDA (Food and Drug Administration) is to ensure the safety of medical devices. This involves evaluating the safety and efficacy of medical products before they can be marketed and used in the healthcare system. By regulating the manufacturing and distribution of medical devices, the FDA aims to protect public health by ensuring that these devices meet applicable safety standards and are effective for their intended use. This responsibility is crucial because medical devices can have direct impacts on patient health and safety, and proper regulation helps to minimize risks associated with their use.

Other roles of the FDA include overseeing the approval of pharmaceuticals and ensuring that food products are safe, but the specific focus on medical devices highlights the agency's commitment to safeguarding public health in that area.

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To assess financial performance of healthcare organizations

To provide healthcare services directly

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