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Framework for Regulatory Oversight of Laboratory Developed Tests (LDTs) - Day 1

Thursday, January 8, 2015, 8:30:00 AM, 8 hours, 30 minutes.

Description: Public Workshop to discuss FDA’s proposal for a risk-based framework for addressing the regulatory oversight of a subset of in vitro diagnostic devices (IVDs) referred to as laboratory developed tests (LDTs).

For more information go to http://www.fda.gov/MedicalDevices/NewsEvents/WorkshopsConferences/ucm423537.htm
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Author: Food and Drug Administration
Runtime: 8 hours, 30 minutes
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Event ID: 15449