February 21, 2023 - February 22, 2023
/ Europe
Meet and Greet Qserve experts at the two-day workshop FDA Pre-Submissions: The Most Valuable Tool in Your US Regulatory Toolbox at RAPS Munich
One of the key tools for market entry in the US is to aid successful FDA submissions is to use the pre-submission process to understand FDA's expectations. Qserve presents at RAPS, FDA Pre-Submissions: The Most Valuable Tool in Your US Regulatory Toolbox.
Tags
Event
FDA
Germany
Global Registration
In-Vitro Diagnostics
Market Access USA
Medical Device Regulations
Medical Devices
Pre Market Requirements
RAPS
Regulatory Affairs
US Agent Service
USA
Workshop