During the roundtable discussion session, the conference hall will be divided into zones. Delegates can choose which zone they would like to join. Each zone will be led by a table moderator and will focus on a different challenge within the medical devices industry.
RT1 – Tackling challenges and harnessing real-world data for medical device companies
Herbert Mauch, Director Clinical Operations EMEA, Cochlear AG
RT2 – Do Notified Bodies’ dedicated programs help or hinder new medical device manufacturers?
Karel Volenec, CEO, ELLA-CS
RT3 -Building a relationship with your study team – how to get good and timely results from everyone included
Pavel Kušnierik, Head of Regulatory Affairs, Contipro
RT4 – PMCF legacy devices: the PMCF Plan, expectations and challenges for obtaining user feedback
Yvonne Hoogeveen, Director Clinical Affairs, Wellinq