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Navigating Regulatory Pathways for In Vitro DiagnosticsNavigating Regulatory Pathways for In Vitro Diagnostics
20 November 2013
Virtual Program

This virtual program provides a basic overview of IVDs with a focus on the regulatory requirements of the US FDA, EU IVDD and MHLW. This program will examine key regulatory requirements and guidelines necessary for effective product development and explain how the intended use of IVDs can define the regulatory pathway for market authorization.

Media Contact

Zachary Brousseau
Senior Manager, Communications
Email: zbrousseau@raps.org
Tel: +1 301 770 2920, ext. 245

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