May 21, 2019 - May 22, 2019
/ USA - Washington, DC
Date: May 21 & 22, 2019
Location: Washington, DC
Mindy McCann, US VP Regulatory Compliance of Qserve Group, is invited as speaker at the 2-days MedTech Intelligence EU MDR Clinical & Post-market Surveillance Strategies.
The EU MDR requires significantly larger amounts and different types of both premarket and postmarket device safety and performance data. In addition to more rigorous clinical information and active collection and analysis of postmarket experiences – for legacy devices as well as new products – new processes and governance will be needed to support this assessment and ongoing file updates. In this highly interactive, practical workshop, companies and notified bodies share strategies and procedures for approaching these massive changes.
For the full program details, please visit the official website.
With offices in the USA, Europe, and China we are an essential partner for medical device manufacturers. With our global team of multilingual consultants, Qserve's expertise and experience provide international support, on a local level.