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What To Watch As EU Clinical Trial Compliance Changes - Food, Drugs, Healthcare, Life Sciences

To print this article, all you need is to be registered or login on Mondaq.com. Earlier this year, industry became more intimately familiar with the clinical trials reporting requirements in the U.S. when, on April 27, the  U.S. Food and Drug Administration sent a notice of noncompliance to Acceleron Pharma Inc. identifying the companys failure to submit study results from a November 2017 trial that tested the efficacy of dalantercept and axitinib, proposed treatments...
Martinh Voss Us Public Health Service Drug Administration Modernization Us Department Of Health Human Services National Institutes Of Health
Source: mondaq.com

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