Archives: Agenda

• Piloting practical tools and workflows for collecting high-quality data across international sites
• Navigating local requirements and global compliance for multi-country observational programs
• Integrating imaging, monitoring, and electronic trial master files to strengthen data integrity and site collaboration

• Balance in-house teams with outsourced or consultant support
• Define key roles from CER writing to PMCF strategy
• Develop career pathways for growing clinical talent pools

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 Proactive management of safety risks in clinical research
Talia Milosevic, Director, Clinical Safety, Surgical Structural Heart, Edwards Lifesciences

RT2 Structuring your clinical team for efficiency and growth
Dr Stephan Theinert, Head Clinical Development, Eyesense

RT3 Strengthening clinical data reliability and assurance in device development
Anna Mayer, Clinical Auditor, TÜV SÜD

RT4 Fostering positive CRO relationships: tips and best practice
Luca Franceschini, Clinical Project Manager, Aboca