February 29, 2024 - March 01, 2024
Join the two-day workshop on US FDA Pre-Submissions led by Lorry Weaver and Christie Hughes
In this 2-day workshop in Rotterdam, The Netherlands, our US FDA experts Lorry Weaver and Christie Hughes will review the multiple types of pre-submissions, or Q-submissions, available to manufacturers and how to leverage these to reduce the time and costs to bring medical devices to market in the U.S.
Medical Device Regulations
Pre Market Requirements
US Agent Service
US Market Access