How many days do you spend to generate the 1st draft of the submission documents? Do you feel pressured due to shorter time schedule and complex scientific information? Along with eCTD structural mastery, writers are required to bring to their task data integration skills, consistent approaches to explanation, and a collaborative spirit. 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. 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.
In this webinar, we’ll showcase the collaborative workflows and powerful content generation that new CoAuthor software 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.
For whom the webinar will be beneficial the most:
- Regulatory Affairs in Pharmaceutical companies and CROs
- Medical Writing team in Pharmaceutical companies and CROs
Speakers:
- Cleagh Arnolds, Associate Director, Commercial and Business Strategy Regulatory Sciences and Medical Affairs at Certara
- Christopher Kutzler, Product Manager at Certara