PANEL DISCUSSION Maximizing market access in Europe: navigating EU MDR and crafting global strategies

  • Addressing complexities of European market access frameworks
  • Leveraging EU MDR compliance to optimize market entry
  • Integration of local and global market strategies
  • Collaborative approaches to overcome regulatory and funding barriers

Moderator
Dave Ribble, Medical Devices Expert, GlobalData

Panelists
Divya Raman, Senior Director of Policy, Intelligence, and Strategy, Teleflex
Jason Neff, Senior Principal Scientific Affairs Specialist, AtriCure
Lisa Griffin Vincent, Chief Regulatory, Quality, Clinical Officer, GT Metabolic

KEYNOTE PANEL DISCUSSION Transforming care: advancing medical devices for a smarter, connected future

Transforming care: advancing medical devices for a smarter, connected future

  • Exploring how emerging technologies are reshaping the design, functionality, and connectivity of medical devices
  • Identifying opportunities for improving patient outcomes by integrating data, diagnostics, and real-time monitoring
  • Addressing challenges in scaling innovation while ensuring safety, interoperability, and regulatory compliance

 

Moderator
Dave Ribble, Senior Consultant, Medical Devices, GlobalData

Panelists
Monika McDole-Russell, Former Senior Director, Global Regulatory Affairs, Medtronic
Kristian Killian, Regional Vice President, VitaTek
Michael Morton, Senior Director of Government Affairs & Policy, Medical Alley
Dr. Nikhil A. Khadabadi, Chief Medical Officer, Eclevar Medtech

Industry Panel Discussion: From Tech to Table – Balancing Digital and Human Touchpoints in the Restaurant

Taking F&B tech from theory to practice through key discussions on:

  • Creating a harmonious service model that empowers guests to choose their preferred way to order and dine
  • How leading hotels are using technology to enhance rather than replace human interactions
  • Real success stories of hotels maintaining service excellence while expanding digital capabilities
  • Strategies for training staff to confidently switch between digital and traditional service modes

Panel Discussion: Navigating updated GCP guidelines: ICH E6 (R3)

  • Highlighting the key changes in ICH E6 (R3) and their practical implications for clinical trial conduct
  • Exploring approaches to implementing new guidelines in diverse trial settings
  • Analysing challenges, opportunities, and interpretations associated with ICH E6 (R3)
  • Sharing actions taken so far to comply with latest updates