What does IVD stand for in the regulatory context?

In the regulatory context, IVD stands for In Vitro Diagnostic. This term refers to medical devices and tests that are performed on samples such as blood, urine, or tissue taken from the body to diagnose diseases, conditions, or infections. In vitro diagnostics play a crucial role in healthcare by enabling the detection and monitoring of various health issues without the need for invasive procedures.

Understanding the definition of IVD is essential for regulatory affairs professionals, as these products are subject to specific regulations and guidelines established by agencies such as the FDA in the United States. The classification and approval process for IVDs is distinct from that of other medical devices, owing to their unique applications and the need for reliable performance to ensure patient safety and effective treatment.