Regulatory Open Forum

I wanted to give you and your team a heads-up on an upcoming workshop that will help you improve your submissions to global health authorities, such as the FDA and EMA. 

Join @Arvilla Trag and you’ll learn how to provide structure and content to Module 3 that will facilitate review and avoid frustrating reviewers. 

She’s planning to share her recommendations for creating data tables, figures that are clean and clearly labeled, and wording that is uncomplicated and easy to read. And while Arvilla will focus mainly on Module 3, her lessons can also be applied to other modules. 

Hope to see you there! Register today.