Global GS1 Healthcare Conference Lisbon, October 2012
|
|
|
- Norah Brooks
- 10 years ago
- Views:
Transcription
1 22 nd Global GS1 Healthcare Conference GS1 Standards - a globally harmonized way to improve patient safety Join a few hundred key stakeholders at the 22 nd Global GS1 Healthcare Conference in Lisbon from 23 to 25 October Learn Share - Network Participants from around the world join the global GS1 Healthcare conferences to: - gather the latest on industry and regulatory developments in automatic identification, traceability and electronic product catalogues - leverage a unique neutral and international platform to network and benchmark with other stakeholders from around the world - learn more about existing supply chain data standards Successfully Bringing Together Supply Chain Stakeholders The Global GS1 Healthcare Conference brings together all related Healthcare supply chain stakeholders to advance the development and adoption of global standards in the Healthcare supply chain. Key stakeholders in the Healthcare supply chain are invited to participate in the global GS1 Healthcare Conference, including representatives from (inter-)governmental bodies and regulators, Healthcare providers, pharmacists, manufacturers, distributors & wholesalers, logistics providers, industry associations, and GS1 Member Organisations representing local communities. 1
2 Week-At A Glance Venue Marriott Lisboa, Avenida dos Combatentes Lisbon, Portugal About GS1 Healthcare GS1 Healthcare is a voluntary, global Healthcare user group leading the Healthcare sector to the successful development and implementation of global standards by bringing together experts in Healthcare to enhance patient safety and supply chain efficiencies. For more information, visit 2
3 Tuesday, 23 October 2012 Draft agenda 8:00 Opening registration and welcome coffee 8:15 9:15 Introduction to GS1 Healthcare - the Global perspective 9:30 11:10 OPENING PLENARY SESSION 9:30 9:50 9:50 10:10 10:10 10:30 10:30 10:50 10:50 11:10 Welcome to Conference João Guimarães, CEO, GS1 Portugal Paul Voordeckers, President Industry Engagement, GS1 Global Office Ministry of Health, Portugal Paulo Macedo - invited INFARMED Eurico Castro Alves, President - invited Unambiguous, standardised and harmonised Unique Device Identification (UDI) Jay Crowley, Senior Advisor for Patient Safety, US FDA The Australian Supply Chain Reform Agenda - Current status and next steps Mark Brommeyer, Manager Supply Chain, NEHTA 11:10 11:40 Coffee break 11:40 13:00 11:40 12:00 12:00 12:10 12:10 13:00 PLENARY SESSION Mc Kinsey report on global standards for Healthcare supply chains Presentation of the Mc Kinsey report on global standards for Healthcare supply chains Katy George, Partner, McKinsey&Co Industry perspective Ajit Shetty, Johnson & Johnson Panel discussion Panelists: Mike Duffy, Vice President, Cardinal Health Ajit Shetty, Johnson & Johnson Katy George, McKinsey&Co 13:00 14:00 Lunch 3
4 13:00 15:00 Working lunch - HPAC (Healthcare Providers Advisory Council) - Andrew Smith, Hospital Sterile Services Unit Manager, St James Hospital, Dublin, Ireland - Tom Pereboom, Project Manager, Utrecht University Medical Center, The Netherlands - Frédérique Frémont, CHI Ballanger, France 14:00 15:00 ASK THE EXPERTS Concurrent breakout sessions 15:00 15:30 Coffee break - Ask the GS1 DataMatrix expert Chuck Biss, Senior Director, AIDC Healthcare, GS1 Global Office - Ask the local Barcoding Expert (in Portuguese) Silvério Paixão, GS1 Portugal 15:30 17:00 PLENARY SESSION Unique Device Identification (UDI) 15:30 15:50 15:50 16:10 16:10 16:25 IMDRF activities and progress on UDI in Europe Fabio Faraulo, Policy Officer, Cosmetics and Medical Devices Unit, Directorate-General Health and Consumers, European Commission - tbc Eucomed s perspective on UDI Mike Kreuzer, Technical and Regulatory Director, ABHI COCIR perspective on UDI Speaker tbc 16:25 17:00 Panel Discussion on UDI 4
5 Wednesday, 24 October :15 8:45 Welcome coffee and MO poster session 8:45 12:30 PLENARY SESSION - Traceability 8:45 9:05 9:05 9:45 EU Commission activities on falsified medicines Stefano Soro Head of Product & Service Safety Unit Directorate General Health & Consumer Update on supply chain stakeholders' activities in the EU: the European Stakeholder Model (ESM) - EAEPC, EFPIA, GIRP, & PGEU Grant Courtney, EFPIA Monika Derecque-Pois, Director General GIRP John Chave, Secretary General PGEU 9:45 10:05 The German securpharm pilot project Christian Riediger, Strategy & Operations Management, Bayer 10:05 10:25 EDQM activities around counterfeiting and traceability François-Xavier Lery, Scientific Officer, EDQM (European Directorate for the Quality of Medicines & HealthCare), Council of Europe 10:25 10:55 Coffee break and MO poster session 10:55 11:15 The Pharmaceuticals Track & Trace System (ITS) in Turkey Serap Malçok Altunakan, Ministry of Health Turkey - invited 11:15 11:35 Developments on Traceability in the US Peggy Staver, Director Product Integrity, Pfizer 11:35 12:30 Panel discussion on Traceability 12:30 13:30 Lunch and MO poster session 5
6 12:30 14:30 Working lunch Public Policy session 13:30 14:30 ASK THE EXPERTS Concurrent breakout sessions 13:30 14:30 - Ask the bedside scanning and Patient ID experts Nilson Malta, Albert Einstein Hospital, São Paolo, Brazil Christian Hay, GS1 GO - How are GS1 Standards developed? Ask the expert Bob Bersani, GS1 GO 14:30 17:00 PLENARY SESSION GDSN 14:30 14:50 14:50 15:10 15:10 15:30 Spain: GDSN Data Crunch in Healthcare GS1 Spain, speaker tbd Abbott Case Study: Implementing GDSN in Australia Dianne Prince, Customer Supply Chain Manager, Abbott Australia EDI and product catalogue in an Irish hospital St James Hospital, Dublin, Ireland, Speaker tbd 15:30 16:00 Coffee break and MO poster session 16:00 16:20 Cook Medical Australia s journey to being EDI compliant Jithendra Nair, Director IT Asia Pacific, Cook Medical 16:20 17:00 Panel Discussion on GDSN 19:30 Networking event 6
7 Thursday, 25 October :00 10:50 PLENARY SESSION Hospital implementation 9:00 9:20 9:20 9:40 9:40 10:00 10:00 10:20 Hospitals implementing GS1 standards why? Feargal McGroarty, Project Manager, NCHCH, St James Hospital and Janice Kite, GS1 GO Improve patient safety and efficiency in the OR Potential savings of 170 million euro in Dutch hospitals Justin Bitter, Head of OR at University Medical Center, Nijmegen, Netherlands The need for barcoding of the single dose Roberto Frontini, President, European Association of Hospital Pharmacists Implementation of barcode scanning in a hospital in Brazil Nilson Malta, Pharmacist, Albert Einstein Hospital, São Paolo, Brazil - 10:20 10:50 Panel discussion on hospital implementation and requirements 10:50 11:20 Coffee break 11:20 13:00 PLENARY SESSION Implementation and CLOSING 11:20 11:40 11:40 12:00 12:00 12:20 Implementing GS1 Standards in Novartis Margarida Alves, Drug Regulatory Affairs Manager, Novartis and Michael Ritter, Novartis Efficiency models in the Andalusian health service supply chain update María Ramírez, Economic Management Directorate, Andalusian Health Service Building a Global Serialization Compliance Management System Lewis Kontnik, Director Brand Protection, Amgen 12:20 12:40 Keynote speaker: Prof Augusto Mateus 12:40 12:50 Welcome to Buenos Aires, April 2013 conference 12:50 13:00 Closing remarks GS1 Healthcare Tri-chairs 13:00 Closing Lunch 7
GS1 Healthcare Provider Advisory Council (HPAC) Feargal McGroarty St James Hospital, Dublin, Ireland HPAC Tri-Chair
GS1 Healthcare Provider Advisory Council (HPAC) Feargal McGroarty St James Hospital, Dublin, Ireland HPAC Tri-Chair About HPAC Formation: December 2010 Objectives: Scope: A forum for sharing and discussing
A European Medicines Verification System
Ensuring patients have access to safe medicines A European Medicines Verification System Fighting counterfeit medicines to ensure patient safety in Europe Speaker: Ms. Monika Derecque-Pois Event: Scientific
European Medicines Verification System (EMVS) Status March 2015
European Medicines Verification (EMVS) Status March 2015 Introduction Grant Courtney Previously a member of the EFPIA Serialisaiton & Coding Steering Team Member of GS1 Healthcare Leadership Team 20 Years
20-21 May 2015, Lisbon, Portugal. Highlights. Speakers:
Speakers: Dr Afshin Hosseiny Chair of the ECA Expert Working Group on GDP, Tabriz Consulting Comply with the new EU GDP Guideline Dr Martin Egger Pharmaserv Dr Daniel Müller GMP/GDP Inspector All participants
Delegated Act on the Detailed Rules for a Unique Identifier for Medicinal Products for Human use, and its Verification
Delegated Act on the Detailed Rules for a Unique Identifier for Medicinal Products for Human use, and its Verification Concept Paper submitted for Public Consultation Response from securpharm e.v. 26 April
A GLOBAL CURE FOR HEALTHCARE
A GLOBAL CURE FOR HEALTHCARE A new and independent report by McKinsey & Company has estimated the benefits - in lives and value - of implementing one single global standard in Healthcare To download the
Building a Serialization Compliance Management System. Lewis Kontnik, Director Brand Protection Amgen Inc. (Oct. 2012)
Building a Serialization Compliance Management System Lewis Kontnik, Director Brand Protection Amgen Inc. (Oct. 2012) About Amgen Amgen discovers, develops, manufactures, and delivers innovative human
Efficient Data Sharing in Healthcare
Efficient Data Sharing in Healthcare More and more efforts are underway in different countries on sharing data among doctors and hospitals in healthcare for achieving higher quality and efficiency of clinical
Transport - track and trace with RFID and latest developments in barcoding
Transport - track and trace with RFID and latest developments in barcoding Thessaloniki, Dr. Knoth 21. April 2012 RFID- Technical data I RFID Radio-Frequency Identification I Uses non-contact identification
Increasing Efficiency in the Healthcare Supply Chain through NEHTA Maria Palazzolo CEO
Increasing Efficiency in the Healthcare Supply Chain through NEHTA Maria Palazzolo CEO Agenda Australia s healthcare system GS1 Australia in healthcare Introducing the National E -Health Transition Authorit
White Paper Healthcare Supply Chain Traceability
Executive Summary This white paper focuses on Healthcare supply chain Traceability, from manufacture to patient, going beyond, for example, what is currently regulated by the US 21 CFR Part 820 and ISO
GS1 Global Update. MIGUEL A. LOPERA, President & CEO, GS1. March 2015
GS1 Global Update MIGUEL A. LOPERA, President & CEO, GS1 March 2015 AGENDA 1. The role of GS1 in an omni-channel world 2. EU 1169 Update 3. The great progress of the GS1 Global Healthcare Initiative 2
How To Help The Global Healthcare User Group (Hug)
HUG Global Healthcare User Group - HUG GS1 s Brand Architecture 2 The global Healthcare User Group - HUG Mission: Lead the healthcare industry to the effective utilization and development of global standards
GS1 STANDARDS & UDI UPDATE SIOBHAN O BARA GS1US
GS1 STANDARDS & UDI UPDATE SIOBHAN O BARA GS1US AGENDA We have the standards. GS1 US Background and Update We have the framework. Unique Device Identification (UDI) We need to move forward. The clock is
Position Paper (II) Healthcare Provider Advisory Council Implementation in hospitals hindered by bar code symbol issues
I. Introduction Towards the end of 2011, GS1 Healthcare established the Healthcare Provider Advisory Council (HPAC) to be the forum for sharing and discussing the practical realities of implementation
Improving Patient Safety and Supply Chain Efficiency with GS1 Standards in HEALTHCARE
Improving Patient Safety and Supply Chain Efficiency with GS1 Standards in HEALTHCARE 1 GS1 STANDARDS IN HEALTHCARE Together, we re making it possible to follow drugs and medical devices from the manufacturer
UNIQUE DEVICE IDENTIFICATION. and in the European Union. Laurent SELLES Senior Coordinator for International Relations Health Technology and Cosmetics
GLOBAL GS1 HEALTHCARE CONFERENCE Copenhagen Denmark 22 October 2014 UNIQUE DEVICE IDENTIFICATION Situation in the International Medical Device Regulators Forum (IMDRF) and in the European Union Laurent
Unique Device Identification Update FDA and GHTF
Unique Device Identification Update FDA and GHTF Jay Crowley Senior Advisor for Patient Safety Food and Drug Administration [email protected] 301-980-1936 UDI Can Improve Visibility Medical device
An enabling volunteering infrastructure in Europe: Situation Trends Outlook
General Assembly Conference: An enabling volunteering infrastructure in Europe: Situation Trends Outlook 14-16 October 2009 Malmö, Sweden What do we mean when talking about an enabling volunteering infrastructure
The Values & Benefits of Using a GDSNData Pool. Prepared by: Anthony Hayes Greg Patterson
The Values & Benefits of Using a GDSNData Pool Prepared by: Anthony Hayes Greg Patterson October 2014 Company Overview Around the world 5 Corporations: USA, Canada, Australia, France, Brazil,(Taiwan-Partner)
Healthcare Coalition on Data Protection
Healthcare Coalition on Data Protection Recommendations and joint statement supporting citizens interests in the benefits of data driven healthcare in a secure environment Representing leading actors in
How companies leverage quality and quality certifications to achieve competitive advantage
How companies leverage quality and quality certifications to achieve competitive advantage Eize de Boer Systems & Services Certification International Business Development Manager Pharma Supply Chain for
Programme. 26 th Global GS1 Healthcare Conference
Programme 26 th Global GS1 Healthcare Conference The power of global standards in healthcare Copenhagen, 21 23 October 2014 Table of Contents Acknowledgements...3 Week at a glance...4 Welcome...5 Agenda...6
training programme in pharmaceutical medicine Regulatory affairs
training programme in pharmaceutical medicine Regulatory affairs INFARMED, Lisbon 19-21 january 2012 Regulatory affairs 19 21 january 2012 LocaL: INFARMED, Lisbon curricular unit Leader: Hélder Mota Filipe,
Takeda UPI Contribution to Conference. Vendor selection process for Serialization and product Tracking. May 2014. Authors: Bahman Didar
Takeda UPI Contribution to Conference Vendor selection process for Serialization and product Tracking May 2014 Authors: Bahman Didar Delivering the Unified Product Identifier Program at Takeda Agenda 1.
Track & Trace. The Distribution Chain to the EU and within the EU
ECA ACADEMY The new GDP and Track & Trace Regulations in Europe Jersey City, NJ (New York City Metro Area), USA July 14-15, 2015 A conference organised by the ECA Academy and the European QP Association
Pharmaceutical Distribution Security Alliance (PDSA)
Pharmaceutical Distribution Security Alliance (PDSA) Our Mission The Pharmaceutical Distribution Security Alliance's (PDSA) mission is to develop and help enact a federal policy proposal that enhances
HOT TOPICS IN F&V BRANCHE
HOT TOPICS IN F&V BRANCHE VERSIE 1a 18 juni 2014 Johan den Engelse Powered by @FICHSC HOT TOPICS IN F&V BRANCHE Frug I Com? VERSIE 1a An unique 18 juni framework 2014 of cooperation involving the Dutch
SMART GOVERNMENT DAYS
SMART GOVERNMENT DAYS Ulaanbaatar Mongolia, May 2-3, 2013 Smart Solutions is about identifying and scaling innovative, ICT-enabled approaches to development challenges. In this 1.5 day event the Cabinet
Delivering a Comprehensive Serialization Traceability Program Peggy Staver - Pfizer
Delivering a Comprehensive Serialization Traceability Program Peggy Staver - Pfizer Overview Pfizer History What it Takes Strategies Organization Solutions Business-as-Usual Summary April 21, 2015 2 Pfizer
GS1 Standards Implementation have a logical order of chronology and complexity GDSN GLN GTIN
Covidien Data Standards Status Healthcare Transformation Group (HTG) Meeting St. Louis, MO May 2, 2012 The real long-term objective Supply Chain Data UDI Clinical Data 2 GS1 Standards Implementation have
The Australian Supply Chain Reform Past, Present and Future
The Australian Supply Chain Reform Past, Present and Future Kate Ebrill Head of National Service Operation and Management GS1 Healthcare Conference Copenhagen, Denmark 22 October 2014 1 National E-Health
GS1 Global Healthcare Conference
Programme GS1 Global Healthcare Conference The Power of Global Standards in Healthcare Mexico City, 21 23 April 2015 Global GS1 Healthcare Conference Mexico City, 21 23 April 2015 Global GS1 Healthcare
Global GS1 Healthcare Conference
Programme Global GS1 Healthcare Conference Imagine one world, one standard, one vision: improving patient safety Budapest, 20 22 October 2015 Global GS1 Healthcare Conference Budapest, 20 22 October 2015
Operations Planning. Bringing Healthcare Supply Chain to Life: The National E-Health Supply Chain Reform Programme and the Australian Experience
Operations Planning Bringing Healthcare Supply Chain to Life: The National E-Health Supply Chain Reform Programme and the Australian Experience Manager Supply Chain (NEHTA) Agenda 1. Australian Healthcare
AGENDA. Food Contact Materials: Working Together for Safety and Innovation in Europe
AGENDA Food Contact Materials: Working Together for Safety and Innovation in Europe Page 2 Conference Food contact materials: working together for safety and innovation in Europe 30 th September 2015 Luxembourg,
Financial Instruments delivering ESI Funds. Lisbon, Portugal 18 January 2016. Preliminary programme. www.fi-compass.eu
Financial Instruments delivering ESI Funds Lisbon, Portugal 18 January 2016 Preliminary programme www.fi-compass.eu Financial Instruments delivering ESI Funds Index Context... 3 Audience/ venue... 4 Language/
2012 GTIN Sunrise Explained IMPLEMENTATION ROADMAP FOR U.S. HEALTHCARE SUPPLY CHAIN MEMBERS
2012 GTIN Sunrise Explained IMPLEMENTATION ROADMAP FOR U.S. HEALTHCARE SUPPLY CHAIN MEMBERS Contents Executive Overview... 4 U.S. Healthcare Industry Sunrise Dates... 5 2012 GTIN Sunrise... 5 Contrast
GS1 Model for Supply Chain Processes in Healthcare,
GS1 Model for Supply Chain Processes in Healthcare, Part I - Framework Issue 1.0, Ratified, Nov-2014 Issue 1.0, November 2014 All contents 2014 by GS1 Page 1 of 46 Document Summary Document Item Current
Track/Trace Solutions. for the Manufacturing Industry
Track/Trace Solutions for the Manufacturing Industry Today s manufacturers, regardless of what they produce, have no choice but to follow private sector and government required mandates. As examples, two
UDI Systems Comparison Report for Tissue Banks December 20, 2013
This UDI Systems Comparison Report for Tissue Banks provides AATB s membership with an overview of three specific labeling capabilities that will likely be approved by the Food and Drug Administration
SMART InTeRneT OF ThIngS
Join us at the SMART InTeRneT OF ThIngS SUMMIT 2012 Manchester United FC Conference Centre, Old Trafford, UK Supported by: November 26-28 2012 The European Commission The Institution of Engineering and
A. Background. In this Communication we can read:
On RFID The Next Step to THE INTERNET OF THINGS Information of the Presidency 2832nd Council meeting, Competitiveness (Internal Market, Industry and Research), Brussels, 22-23 November 2007 A. Background
Global Data Synchronisation Network User Group Charter
Global Data Synchronisation Network User Group Charter 28 October 2008 Version 3.0 Page 1 GDSN USER GROUP CHARTER AND MEMBERSHIP CRITERIA... 3 GDSN USER GROUP CHARTER AND MEMBERSHIP CRITERIA... 3 GDSN
NEOH workshop and 3 rd management committee
Trans-Domain COST Action TD1404 (NEOH) NEOH workshop and 3 rd management committee Faculdade de Ciências Médicas/Nova Medical School (www.fcm.unl.pt) 18 th and 19 th January 2016 This NEOH workshop (in
Unique identification of pharmaceuticals in Austria
Unique identification of pharmaceuticals in Austria From the national Pharmazentralnummer to an international Global Trade Item Number Stefan Sabutsch GS1 Healthcare Conference Vienna 2009-03-19 Original
Cook Medical Australia s journey to being EDI compliant
Cook Medical Australia s journey to being EDI compliant Presented by Jithendra Nair, Director IT Asia Pacific, Cook Medical, Lisbon Update October 2012 Cook Medical General Information Cook Medical (Cook)
European Cluster Matchmaking Event Brussels, Belgium. Call for Expression of Interest
European Cluster Matchmaking Event Brussels, Belgium organised in the context of the European Cluster Conference 2014 set up by the European Commission s Enterprise and Industry Directorate-General October
GS1 Healthcare Reference Book
GS1 Healthcare Reference Book 2013/2014 Table of Contents Opening Standardised Data for Safer Healthcare & Acknowledgements 3 Introduction Leading the Way for Traceability 4 Argentina ANMAT Marking the
SATO Healthcare Solutions
SATO Healthcare Solutions Barcode, RFID, Printers, Tags, Labels Patient Wristbands, Scanning Solutions and Software www.satoamerica.com Hospitals and clinics Examination centers Clinical laboratory centers
SPONSORSHIP OPPORTUNITIES
SPONSORSHIP OPPORTUNITIES Bangkok, Thailand Thursday 19 th March Sydney, Australia Tuesday 19 th May Seoul, Korea Tuesday 24 th March Shanghai, China Thursday 28 th May Mumbai, India Tuesday 12 th May
SEBP2015. S i n o - E u r o B i o P a r t n e r i n g 中 欧 生 物 医 药 项 目 合 作. Industry Insight Innovation Fostering Bio-Investment Roadshow & Partnering
Thursday May 14 th, 2015 Shanghai, China a S i n o - E u r o B i o P a r t n e r i n g 中 欧 生 物 医 药 项 目 合 作 Industry Insight Innovation Fostering Bio-Investment Roadshow & Partnering INTRODUCTION A partnering
EDQM Certificates of Suitability: Cooperation Among Inspectorates in Europe And Beyond
EDQM Certificates of Suitability: Cooperation Among Inspectorates in Europe And Beyond 14 th International Conference of Drug Regulatory Authorities Pre-ICDRA Meeting Dr Susanne Keitel European Directorate
European Medicines Verification System (EMVS) European Pack Coding Guidelines
European Medicines Verification System (EMVS) European Pack Coding Guidelines June 2013 Revision History V1.0 June 2008 Initial Release V1.1 June 2008 Amended some typographical errors, added extra detail
Drug Distribution Management Policy in Korea
Drug Distribution Management Policy in Korea Regarding introduction of Drug Serial Number System (Serialization) Ministry of Health and Welfare Drug Distribution Management Policy Overview Policy Objectives
Investors' Access. Market. Strategic. Forum. Open. E-Health PROGRAM 2015. Alliance. Innovation PRELIMINARY. Management
OCTOBER 5-6, 2015 PARIS, FRANCE 6 th EDITION THE LEADING PARTNERING MEETING IN OPEN INNOVATION FOR LIFE SCIENCES CONFERENCES EXHIBITION HALL ONE-ON-ONE PARTNERING MEETINGS NETWORKING Open PRELIMINARY PROGRAM
Rx-360 White Paper on Traceability Data Exchange Architecture
Rx-360 White Paper on Traceability Data Exchange Architecture 14 March 2015 Introduction and Scope of Rx360 TDEA White Paper With the quickening pace of global pharmaceutical regulatory drug serialization
LANDWELL. Solicitors. Life Sciences Unit
LANDWELL Solicitors Life Sciences Unit LANDWELL Solicitors Life Sciences Unit Our Practice Landwell Solicitors is a leading firm of business lawyers providing legal solutions to businesses in the Life
FCT PhD Programme Medicines and Pharmaceutical Innovation (i3du)
FCT PhD Programme Medicines and Pharmaceutical Innovation (i3du) Course BioPharmaceuticals and Advanced Therapies 28-2 September/October 2015 - Auditorium The FCT PhD Programme in Medicines and Pharmaceutical
IFA-Coding-System Transport Logistics Specification. Automatic identification of transport units in the pharmaceutical supply chain
IFA-Coding-System Transport Logistics Specification Automatic identification of transport units in the pharmaceutical supply chain Version: 1.00 Date of issue: December 2012 Table of Contents 1 Foreword
EU-US Open Skies: competition and change in the worldwide aviation market
In co-operation with the German Aviation Research Society (G.A.R.S) Second Airneth Annual Conference 17, 18 April 2008 Crowne Plaza Hotel, The Hague The Netherlands CONFERENCE PROGRAM EU-US Open Skies:
116th Annual Convention
116th Annual Convention Date: Saturday, October 18, 2014 Time: 10:30 am 12:00 pm Location: Austin Convention Center, Room 19AB, Level 4 Title: Activity Type: Speaker: Understanding the Drug Quality and
Discussion paper on global harmonization of the traceability system for drugs with globally harmonised barcodes
Purpose The purpose of this paper is to facilitate the discussions for a transition toward a globally harmonised barcoding system for pharmaceuticals in China, using GS1 global standards and building on
Doctoral/ Graduate Education in Asia and Europe. EAHEP Workshop 1 Programme
Doctoral/ Graduate Education in Asia and Europe EAHEP Workshop 1 Programme Dates and venue EAHEP Workshop on Doctoral/ Graduate Education: 40-45 Asian and EU participants 8-9 December 2008, at the EC Delegation
To learn more, visit us here:
To learn more, visit us here: Event details: Date: 19 November 2015 (Thursday) Time: 9:15am 6pm Venue: S221, Hong Kong Convention and Exhibition Centre, Wanchai Time 8:30am 9:15am 9:15am 9:25am 9:25am
By Natalia Wilson, MD, MPH
White Paper The value of unique device identification across healthcare By Natalia Wilson, MD, MPH Executive summary The Unique Device Identification (UDI) System Proposed Rule was published by the U.S.
RESPIRO Conference on Socially Responsible Procurement
RESPIRO Conference on Socially Responsible Procurement 3-4 December 2007, Lille, France Final Invitation and Programme Endorsed by: RESPIRO Responsibility in Procurement Welcome On behalf of the City of
The Drug Supply Chain Security Act: Readiness and Implementation Update
The Drug Supply Chain Security Act: Readiness and Implementation Update Connie Jung, RPh, PhD U.S. Food and Drug Administration Center for Drug Evaluation and Research Office of Compliance Office of Drug
Working Group Meeting of the
Working Group Meeting of the COMMUNITY OF PRACTICE ON HUMAN RESOURCE MANAGEMENT 28-29 May 2015 Zagreb (Croatia) Draft Discussion Paper and Agenda The role of competencies in professionalising civil services
European Non-Wood Forest Products (NWFPs) Network COST Action FP1203
1 European Non-Wood Forest Products (NWFPs) Network COST Action FP1203 1 st Workshop and 2 nd Management Committee Meeting Lisbon, Portugal 20. - 21. June 2013 Local organizers: Margarida Tomé and Luis
SOUTH-WEST EUROPE 21
21 SOUTH-WEST EUROPE SOUTH-WEST EUROPE Croatia, Cyprus, Greece, Italy, Malta, Portugal, Slovenia, Spain Access to medicines and medical devices in Mediterranean EU Member States As members of the EU, all
How To Prepare For A Gfmd Meeting
The GFMD Forum meeting Stockholm 14-16 May 2014 Proposed set up at the meeting Timing and venue The 2014 GFMD Forum meeting will be held in Stockholm 14-16 May 2014. The meeting will take place at Münchenbryggeriet
ACCORD PROJECT FINAL RESULTS OF THE. 2 nd June, 2015. Rafael Matesanz, on behalf of the ACCORD consortium. Director
FINAL RESULTS OF THE ACCORD PROJECT 2 nd June, 2015 Auditorium MUTUA MADRILEÑA Foundation, MADRID Director Rafael Matesanz, on behalf of the ACCORD consortium Achieving Comprehensive Coordination in Organ
Türkiye İlaç ve Tıbbi Cihaz Kurumu
w w w. t i t c k. g o v. t r TURKISH MEDICINES AND MEDICAL DEVICES AGENCY Gulsen ONER, Pharm. M.Sc. Melda KECIK, Pharm. M.Sc. WHO Technical Briefing Seminar, November 2014 OUTLINE I. About Turkey II. About
Skills for a lifetime towards a future proof VET
Skills for a lifetime towards a future proof VET 16-17 January 2016 Amsterdam Programme Introduction The conference on vocational education and training (VET) to be held in the framework of the Dutch EU
The EFPIA Disclosure Code: Your Questions Answered
The EFPIA Disclosure Code: Your Questions Answered Working together: why do the pharmaceutical industry and healthcare professionals work together? 1 Why does industry pay health professionals to provide
Second Mares Conference Abstract Submission Guidelines
Second Mares Conference 1. Introduction 2 2. Abstract Submission & Conference Proceedings 2 3. Conference Programme 2 4. How to submit an abstract? 3 5. Oral Presentation Guidelines 4 6. Exhibition Guidelines
European Federation of Pharmaceutical Industries and Associations (EFPIA) HCP/HCO Disclosure Transparency Requirements Methodology Note for Shire
European Federation of Pharmaceutical Industries and Associations (EFPIA) HCP/HCO Disclosure Transparency Requirements Methodology Note for Shire Contents 1. Overview of the EFPIA Requirements... 3 2.
Main Conference Agenda
Sponsored by: (Co-located with Bioequivalence: Intersection between Science & Regulatory Conference) Main Conference Agenda Day One Wednesday, November 5 th, 2014 7:30 Registration Opens & Continental
K-Series Guide: Guide to digitising your document and business processing. February 2014 LATEST EDITION
K-Series Guide: Guide to digitising your document and business processing February 2014 LATEST EDITION Kefron are the Document Kefron & simplifies the document and Information information management world
Clinical Trial Logistics
BOOK BY 31ST MARCH TO SAVE 100 SMi presents the 8th conference and exhibition series... Clinical Trial Logistics 21ST - 22ND MAY 2014 MARRIOTT REGENTS PARK LONDON, UK EUROPE'S LEADING CLINICAL TRIAL LOGISTICS
THE PRESIDENCY LAPSSET CORRIDOR DEVELOPMENT AUTHORITY DIRECTOR GENERAL / CHIEF EXECUTIVE OFFICER S OFFICE
LAPSSET CORRIDOR DEVELOPMENT AUTHORITY DIRECTOR GENERAL / CHIEF EXECUTIVE OFFICER S OFFICE Chester House, 2 nd Floor Phone: +254 (0) 20-2219098 P.O. Box 45008 00100 Fax: +254 (0) 20-2218968 Koinange Street
Invitation to Host Academy Event
Invitation to Host Academy Event You are invited to host a conference or congress of the Future Academy. If you are interested in serving as host, please complete and sign the attached application form,
8 th European Quality Conference. Draft Programme. 1 st & 2 nd October 2015 Esch-Belval, Luxembourg
8 th European Quality Conference Strengthening the capacity of public in tackling current and future challenges - Public as part of the solution 1 st & 2 nd October 2015 Esch-Belval, Luxembourg Draft Programme
GMP and QMS Regulation in Japan
GMP and QMS Regulation in Japan Tomiko Tawaragi Chief Safety Officer Pharmaceuticals and Medical Devices Agency (PMDA) August 2 nd, 2014 1 st Brazil-Japan Seminar GMP/QMS GMP : Good Manufacture Practice
YOUR EUROPE YOUR FUTURE
EUROPEAN UNION European Commission Committee of the Regions Programme YOUR EUROPE YOUR FUTURE Youth debates for tomorrow's Europe Brussels 18-20 January towards the Rome Youth Summit Programme YOUR EUROPE
USER MEETING 2013 21-22 NOVEMBER. Partnership Packages
USER MEETING 2013 21-22 NOVEMBER Partnership Packages Australian Synchrotron User Meeting 2013 The Australian Synchrotron invites you to partner with the 2013 User Meeting. Our synchrotron user community
