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March 2015
POLICY AND ADVOCACY
IDSA Responds to NIH on Proposed Regulatory Process for Multi-Site Research Trials

IDSA submitted comments to the National Institutes of Health (NIH) in response to its proposed draft policy to streamline the regulatory process of multi-site clinical trials while maintaining research participant protections.  The policy would require all domestic NIH-funded multi-site trials to use a single institutional review board (IRB).  IDSA applauded the draft policy but also noted key questions for NIH to consider as it moves forward with finalizing the policy.

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