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. Our solution enriches Microsoft Word with three purpose-built capabilities: broad template selection, structured content authoring, and behind-your-firewall generative AI that’s specialized for the life sciences.
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.
웨비나 참여 권장 대상:
- Regulatory writers/Medical Writers
- Regulatory Affairs
- Other Applicable Writers
발표자
- Rico Fujita, Solution Consultant, Certara
