As a direct and sole result of the outbreak of the coronavirus disease (COVID-19) and due to circumstances beyond our control, DIA announced last week that it has decided to change the format of the upcoming Medical Affairs and Scientific Communications meeting from “face-to-face” (in-person) to entirely virtual.

For more information, please review the list of Frequently Asked Questions.

*Short Course requires separate registration

In today’s regulatory environment, authors are routinely faced with writing numerous regulatory submission documents involving highly complex studies with overwhelming amounts of data. It is therefore imperative to develop documents that clearly convey the intended key messages to facilitate agency review. This short course will provide an overview of lean authoring, with discussion on the benefits and challenges of this approach. Hands-on activities will offer practical solutions to reduce content redundancy and to improve clarity of regulatory documents, with a focus on key messages. Strategies to help lean authoring succeed at your organization will also be discussed.