On May 6, 2024, the FDA published its highly anticipated final rule, which was formally published in the Federal Register on May 6, revising the regulatory definition of an IVD product to explicitly capture IVDs manufactured by laboratories.
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Leveraging the power of technology to improve early detection, monitoring, and management of the glaucoma has been a critical factor. TheHealthSite.com
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/PRNewswire/ MCRA, the leading privately held independent medical device, diagnostics, and biologics Clinical Research Organization (CRO) and advisory firm.