Faced with more (and more complex) clinical research than ever before, regulatory writers are facing new demands. 各ライターは、eCTDの構造を完全に理解するとともに、データ統合スキル、一貫した説明アプローチ、そして他部門との協働スキルを日々発揮する必要があります。With more to produce, and less time to produce it, the right technology is a must.
Discover that technology in CoAuthor from Certara. CoAuthor provides transparency, consistency, and collaboration to allow regulatory writing teams to accelerate the drafting and submission of quality and compliant regulatory documents. このソリューションは、Microsoft Wordに3つの薬事・メディカルライティング専用機能を追加します。(1)幅広いテンプレート選択、(2)構造化コンテンツのオーサリング、(3)ライフサイエンスに特化した、貴社のファイアウォール内で使用できるGPT機能です。
In this webinar, we’ll showcase the collaborative workflows and powerful content generation that CoAuthor enables. You’ll see the software up close, and learn how the regulatory writing and document quality service teams at Certara are benefiting now, and stand ready to extend your team with their expertise.
講演者
Cleagh Arnolds, Associate Director, Commercial and Business Strategy Regulatory Sciences and Medical Affairs at Certara
Christopher Kutzler, Product Manager at Certara
