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Upcoming Meetings: FDA/industry IVD Roundtable

This article was originally published in The Gray Sheet

Executive Summary

FDA/industry IVD Roundtable: Three-day meeting planned for March or April in Baltimore area to discuss 510(k) requirements for in vitro diagnostics. Participants will include the Health Industry Manufacturers Association, the Medical Device Manufacturers Association, the Independent Reagent Manufacturers Association and representatives from FDA's Center for Devices and Radiological Health and Center for Biologics Evaluation and Research...
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