HUG Meeting 13 - 15 September 2005 , Brussels
Presentations
Day 1 - 13th September 2005
- Introduction to the HUG, Miodrag Mitic, GS1
- HUG Work Plan, Ulrike Kreysa, GS1
- HUG work team: Membership, Volkar Zeinar, B.Braun
- HUG work team: Regulatory Affairs, Jackie Elkin, Medtronic
- HUG work team: Standards Implementation, Tom Werthwine, Manager, AIDC Technology and Industry Standards, Johnson & Johnson
- HUG work team: Standards Development , Peter Tomicki, Baxter
- HUG work team: Business Case, Ed Dzwill, Johnson & Johnson Pharma
- HUG work team: Communication & Coordination, Rich Hollander, Pfizer
Day 2 - 14th September 2005
- The HUG - Mission and Vision, Rich Hollander, Pfizer
- Counterfeit Medicines, Dr. Hans-Georg Wagner, Head of Unit Communications and Networking, European Medicines Agency (EMEA), London
- Strategies to Combat Counterfeit Activities in the EU, Sabine Atzor, European Commission, Enterprise and Industry Directorate-General, Consumer Goods, Unit F2 Pharmaceuticals, Brussels
- Dr. Marianne Takki, European Commission, Public Health Directorate, Health Strategy, Brussels (Presentation not available)
- Food and Drugs Administration (FDA) Update, Michelle Limoli, Associate Director, Office of International Programs U.S. Food and Drug Administration (FDA), Washington, USA
- The drugs tracking system in Italy, Dr. W. Bergamaschi, Director General for Information Science System and Statistics, Italian Ministry of Health, Rome
- Developing Policy On Machine Readable Codes On Medicines In England, Prof. David Cousins, Head of Safe Medication Practice, NHS National Patient Safety Agency, London
- Product Identification, Jesus Gavira Sanchez, General Administration of Economic Management, Regional Healthcare Service Area of Andalusia
- Overview of GS1 Healthcare activities in Europe, Jim Bracken, CEO, GS1 Ireland
- Overview of GS1 Healthcare activities in North America, John Roberts, Director Healthcare, GS1 US
- Overview of GS1 Healthcare activities in Japan , Yamoto Miyahara, General Manager, GS1 Japan
Day 3 - 15th September 2005
- Standards Development - Feedback from Plenary Session, Peter Tomicki, Baxter
- Regulatory Affairs - Feedback from Plenary Session, Jackie Elkin, Meditronic