4th Annual Medical Device and Diagnostic Regulatory Affairs Conference 12th – 14th November Frankfurt, Germany Distinguished Speakers Regulatory Affairs European Market (MDR/IVDR) Inge Vandenbussche Director Regulatory Affairs EMEA & AR PRRC Nebojsa Serafimovic Assessor, CIE-Member Vesna Kostanjevecki VP of Clinical and Regulatory Development Benno Uennigmann Senior Manager Policy & Advocacy Breda Kearney Clinical Regulatory Lead Kiran Jose Sr Regulatory Affairs Specialty Annette Van Raamsdonk Lead Quality Regulatory Affairs Hamidreza Alidousti Orthopaedic and Dental Team Manager John Josef Molenda Co-Chair of Healthcare & Life Sciences Group Roberto Girardi Senior Director, Head of Privacy Enablement Adam Gregory Head of Regulatory Affairs Dr Francesca Bevilacqua IVD Team Leader Liz Gommans Technical Professional David Boutellier Co-Founder & CEO Dr. Jörk Zwicker Partner Dr. Sebastian Höpfner Partner Regulatory Affairs Global Markets (USFDA, APAC, EMEA REGIONS) Carine Cochereau Vice President Regulatory Caroline Alexander Director Of QA/RA Priya Bhutani Founder and CEO Dr. Susana de Azevedo Wasch Vice President Quality Management & Regulatory Affairs Venkata Harish Chengalvala Sr. RA Specialist - Environmental Compliance and Regulatory Intelligence Sandi Schaible Executive Director Analytical Chemistry and Regulatory Toxicology Ella Helgeman Regulatory and Quality Director Anne-Gabrielle Haie Partner Kirsten Eickho Manager Regulatory Affairs Dr Pavan Kumar Malwade Principal Engineer - Regulatory Affairs Katie Logan Regulatory Affairs Manager Jocelyn Zhu Chief Operating Officer Aouda Ouzzaa Senior regulatory affairs manager level head QA-PRRC Adam Gregory Head of Regulatory Affairs