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人工智能驱动的法规撰写软件 — 日本客户的常见问题 【日本网络讲座】

网络研讨会

Faced with more and more complex clinical research than ever before, regulatory writers are facing new demands. Along with eCTD structural mastery, writers must bring to their task data integration skills, consistent approaches to explanation, and a collaborative spirit.  

AI-powered writing software, CoAuthor™, helps your writing team to accelerate the drafting and submission of quality and compliant regulatory documents. 我们的解决方案立足于 Microsoft Word,且独具匠心地融入了三项核心功能,助力生命科学领域的法规协作团队:丰富的的模板库、结构化内容创作以及专为生命科学领域设计的领先的防火墙AI技术。

Since we launched CoAuthor, we receive many questions from pharma’s regulatory writing teams about the functions and available templates. In the webinar, we will introduce the writing technologies along with frequently asked questions so that your team can streamline the current complex writing process. 

网络研讨会对谁最有帮助: 

  • Regulatory writers/Medical Writers
  • Regulatory Affairs
  • Other Applicable Writers

主讲人: 

  • Rico Fujita, Solution Consultant, Certara
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