Presentations - Day 2 - Wednesday

Plenary session - Pharmaceutical traceability from manufacturer to patient

• GS1 standards as the foundation for implementing the EU FMD - Dirk Van Den Wouwer, Serialization and end-to-end traceability leader EMEA, Johnson & Johnson
• EMVO plus NMVO presentation (Bulgaria) - Andreas Walter, Coding & Serialisation Director, EFPIA & Director General a.i., EMVO; Illiana Paunova, Executive Director, Bulgarian Medicines Verification Organisation (BgMVO)
• What is next after the results of implementing GS1 Pilot in the Public Health Supply Chains - Muhammad Tariq, Country Director, Pakistan, USAID | Deliver Project and John Snow, Inc., Health LogisticsDrug Regulatory Authority of Pakistan (DRAP)
• Pharmaceutical serialization and traceability system in Korea - JeongHwa Oh, Deputy Manager, Pharmaceutical information management department, Korea Pharmaceutical Information Service (KPIS)
• EU Falsified Medicines Directive (FMD) and Beyond – Implementation Challenges for a Manufacturer - Stefan Artlich, Director Product Tracking and Authentication, Bayer, Germany
• Implementation traceability system - Christina Kögler, Packaging Engineer, Bausch & Lomb
• The traceability regulation in US and roadmap towards implementation - Peggy Staver, Packaging & Delivery Systems, Pfizer; Scott Mooney, Vice President, Distribution Operations, McKesson; Jeff Denton, Sr. Director, IT Global Secure Supply Chain, AmerisourceBergen Corp

Ask the expert sessions

1. Pharmaceutical subjects

• Shared packs, coding status/NTIN to GTIN - Joan Cahill, Director, Packaging & Delivery Systems, Pfizer; Grant Courtney, Manager, Falsified Medicines Directive Project, GSK
• DataMatrix/HRI - Chuck Biss, Senior Director, AIDC Healthcare, GS1 Global Office
• Traceability/serialisation - Peggy Staver, Director, Product Integrity, Pfizer; Scott Mooney, Vice President, Distribution Operations, McKesson; Jeff Denton, Sr. Director, IT Global Secure Supply Chain, AmerisourceBergen Corp.; Craig Alan Repec, Senior Manager, Supply Chain Visibility, EPCIS & RFID, GS1 Global Office
• IDMP/FMD in hospitals - Christian Hay, Senior consultant, GS1 Global Office; Rob Moss, Director of Professional Development, EAHP

2. Medical Device, Identification and Data Management - Linda Sigg, Associate Director for Informatics, Office of Surveillance and Biometrics FDA Center for Devices and Radiological Health (CDRH), U.S. FDA; Terrie Reed, MS Industrial Engineering, Senior Advisor for UDI Adoption, U.S. FDA; Georg Keller, Manager Regulatory Affairs/Labeling Coordinator B. Braun/Aesculap; Jackie Elkin, Global Regulatory Affairs, Global Process Owner Standard Product Identification, Medtronic; Peter Alvarez, Senior Director, Identification and Data Strategy, Healthcare, GS1 Global Office