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FDA To Participate In Six More GMP Inspections In EU, Weighs Sampling

机译:FDA将参加欧盟的六项GMP检查

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摘要

At the 12th negotiating round for a Transatlantic Trade and Investment Partnership, regulators from both sides agreed they would continue their work aimed at collecting data which will ultimately allow them to decide whether U.S. and EU inspection systems for Good Manufacturing Practices (GMP) in pharmaceutical factories are equivalent, according to a European Commission Report released on March 23.
机译:在跨大西洋贸易和投资伙伴关系的第12轮谈判中,双方监管机构同意他们将继续开展旨在收集数据的工作,这些数据最终将使他们能够决定美国和欧盟是否对制药厂的良好生产规范(GMP)检查系统根据3月23日发布的欧盟委员会报告,这是等效的。

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