In our pursuit to bring medicines to patients faster, we must continuously evolve alongside an endlessly changing regulatory landscape. For Regulatory Professionals, this translates into increased complexity, additional requirements, and less time for submission preparation. This session will explore the past and future of regulatory submissions, from the perspective of the Regulatory Professional. Together, we will discuss how both processes and technologies are evolving.
Learning Objectives:
Understand the historical and present state of regulatory submissions in terms of content, technology, and evolution of regulatory pathways.
Appreciate the industry trends towards the future of submissions with the intent of translating that information to their own organizations.
