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What does the FDA’s final rule on LDTs change? The rule makes it explicit that in vitro diagnostics (IVDs) that are manufactured by clinical laboratories—i.e., laboratory-developed tests (LDTs)—are considered devices under the Federal Food, Drug, and Cosmetic Act (FDCA). IVDs are tests performed on samples such as blood or tissue that have been taken from the human body. LDTs are ...
Enhanced Reports ARUP's enhanced laboratory test reports are available for certain tests as an alternative to traditional text-based charts.
Please provide your email address to receive an email when new articles are posted on . The glaucoma surgery procedure profile has expanded, with many choices for the surgeon to utilize to assist in ...
The cost of bariatric surgery, as well as how much weight they can be expected to lose following the procedure, strongly influence patient preference for the type of operation they chose, new survey ...
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