This presentation will discuss the use of a RIM platform to manage regulatory submissions for medical devices. It will cover the pitfalls of the current landscape and will show ways to optimize this process leveraging AI. There will be use cases to see how companies are leveraging this technology to streamline this process.
Learning Objectives:
Understand the current medical device submission management process
Discuss the pitfalls of the current process.
Discover how companies are leveraging technology to streamline this process.
Uncover how AI can be utilized to expedite this process.
