翻译技术速递Video: Transitioning to Clinical Trials Regulation
视频：过渡到临床试验法规
The transition of ongoing studies to the EU Clinical Trials Regulation (CTR) is a heavily administrative process that takes up to three months. Trial sponsors can avoid it by acting before October 16, 2024, to select the expedited procedure. Discover how you can avoid the burden of a full process and how Lionbridge can assist with any expedited clinical trial translations for your transitioning application. Watch our video to learn more.
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Need assistance with your Life Sciences translation projects? Lionbridge has decades of experience with clinical trial translation services, content generation, and more. We’re also industry leaders in offering Generative AI services.
正在进行的研究向欧盟临床试验法规（CTR）的过渡是一个需要长达三个月的行政管理过程。试验申办者可以通过在2024年10月16日之前采取行动来选择快速程序来避免它。了解如何避免整个流程的负担，以及Lionbridge如何帮助您为过渡申请提供快速的临床试验翻译。观看我们的视频了解更多信息。
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生命科学翻译项目需要帮助吗？Lionbridge在临床试验翻译服务、内容生成等方面拥有数十年的经验。我们也是提供Generative AI服务的行业领导者。
以上中文文本为机器翻译，存在不同程度偏差和错误，请理解并参考英文原文阅读。
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