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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.
Leveraging the power of technology to improve early detection, monitoring, and management of the glaucoma has been a critical factor. TheHealthSite.com
/PRNewswire/ -- MCRA, the leading privately held independent medical device, diagnostics, and biologics Clinical Research Organization (CRO) and advisory firm...
/PRNewswire/ -- The organizers of the Advanced Lateral Flow Conference (ALFC) 2024 are excited to announce that the full conference agenda is now available for...
The organizers of the Advanced Lateral Flow Conference (ALFC) 2024 are excited to announce that the full conference agenda is now available for download. This year's conference, set to take place on February 12-14, at the Hard Rock Hotel San Diego,...