Editorial ArticleClinical Diagnostics
What does the FDA’s final rule on LDTs mean for clinical laboratories?
Explore how the FDA’s final rule on LDTs will affect how clinical laboratories conduct their operations
The Food and Drug Association (FDA) is an agency within the U.S. Department of Health and Human Services. Among other things, it is responsible for ensuring the safety, effectiveness and quality of drugs, vaccines and other biological products, and medical devices.
Explore how the FDA’s final rule on LDTs will affect how clinical laboratories conduct their operations