二月 29, 2024 - 三月 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
US Market Access