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USA: Draft Guidance re In Vitro Companion Diagnostic Devices

17/7/2011

This draft guidance was issued for comment on 14th July 2011.  This guidance is intended to assist:

  1. sponsors who are planning to develop a therapeutic product that depends on the use of an in vitro companion diagnostic device (or test) for its safe and effective use, and
  2. sponsors planning to develop an in vitro companion diagnostic device that is intended to be used with a corresponding therapeutic product.

Author: Greer Deal, Director of Global Regulatory Services (GRS)

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