pharmaceutical logistics 2017
TRANSCRIPT
www.pharmaceutical-logistics.comRegister online or fax your registration to +44 (0) 870 9090 712 or call +44 (0) 870 9090 711
@SMIPHARM
CHAIRS FOR 2017:• Tony Wright, CEO, Exelsius• Bob Hayes, Director, Seer Pharma
EXPERT SPEAKER PANEL INCLUDE:• Glen Hodgson, Head of Healthcare, GS1• Jim Shaw, Head of Sourcing & Supply, AstraZeneca• Rebecca Jackson, VR/IWR Manager,
Randomisation and Trial Supply Services, Johnson and Johnson
• Jasmin Hellwig, Senior Comparator Specialist, Merck, Sharp and Dohme
• Mark Champ, Logistics Supervisor, GSK• Gaetano Carubia, TSMS Control Strategy & Process
Monitoring Consultant, Eli Lilly• Chris Wallace, Senior Director International Supply
Chain, Sanofi Genzyme• Jason Breakwell, Vice Chairman, TAPA
KEY BENEFITS FOR 2017:
• Gain key regulatory updates and effects of the newly-implemented EU GDP Guidelines
• Explore the impact of the Falsified Medicines Directive to the supply chain
• Find out more about the latest innovations in technology and their applications in clinical trial logistics
• Discuss approaches to supply chain visibility and anti-counterfeiting technology
• Discover time and temperature controlled risk strategies
• Join insightful discussions on pharmaceutical logistics in emerging markets
18TH - 19TH
MAY 2017
COPTHORNE TARA HOTEL, KENSINGTON, LONDON, UK
SMi Presents the 11th annual conference and exhibition on…
Pharmaceutical
Logistics Transforming supply chain visibility and management
BOOK BY 31ST JANUARY TO SAVE £400BOOK BY 28TH FEBRUARY TO SAVE £200BOOK BY 31ST MARCH TO SAVE £100
Pharmaceutical Logistics Day One | Monday 18th May 2017 www.pharmaceutical-logistics.com
08.30 Registration & Coffee
09.00 Chairman’s Opening RemarksTony Wright, CEO, Exelsius
MEETING THE DEMANDS OF TEMPERATURE REGULATION AND WAREHOUSING
09.10 Update on IATA’s Pharma Handling Certification Program CEIV• discussion on how to improve the level of competency,
operational and technical preparedness for temperature-sensitive air freight shipments
•WhattheIATACEIVPharmacertificationprogramentailsand how it can revolutionise your distribution strategy
• How to approach the issue of the pharma cargo community collaboration and its present global status
• What the organisation does, how it does it and why it does itFrancisco Rizzuto, Cargo Specialist Manager, IATA (International Air Transport Association)
09.50 Shipping GSK’s Crown Jewels, frozen by sea• How to ship high value discovery samples from Spain to the US• Saving more than £250K- how we accomplished this•Experienceofdampingthetemperaturefluctuation
associated with the defrost cycle for the reeferMark Champ, Logistics Supervisor, GSK
10.30 Morning Coffee
11.00 Optimising warehouse management • Moving from 20th to 21st century in material management
and storage• Technology enabled solutions to ensure accuracy of
inventory, compliance and control• Three joint changes – new facility, new skills and new
improved process Jim Shaw, Head of Sourcing & Supply, AstraZeneca
11.40 Qualification of ocean shipments of temperature sensitive products•Casestudyonthequalificationexercisewearecurrently
working on• Brief background into containers and affect they have on
shipping•Howtodeveloparobustqualificationstrategy-thesteps
we took to ensure this• An example of an ocean shipping route and loading plan• Examples of shipping studies, Process Flow and good
practices when monitoring, shock/ vibrationGaetano Carubia, TSMS Control Strategy & Process Monitoring Consultant, Eli Lilly
12.20 Networking Lunch
CHALLENGES WITHIN CLINICAL TRIAL LOGISTICS
13.30 The Impact of Innovation… on the patient, the clinical trial,
the technology, and you
• The increased use of technology in healthcare and what it
means for the patient
• What exactly is ‘innovation’ when applied to clinical
research, and are we really doing it?
• The technical implications of innovation
• How to embrace change and be an Innovation Leader
Rebecca Jackson, Senior Manager, Solution Architecture,
Johnson and Johnson
14.10 Leveraging demand forecasting to optimise supply flow
• Approaches to effective demand planning strategies
• Methods to facilitate short term supply mitigation
• Offshoring of supply chain processes to Bangalore
Juan Francisco del Castillo Mazzini, Senior Supply Chain
Consultant, Novo Nordisk
14.50 Afternoon Tea
15.20 Sourcing comparators for Chinese clinical supplies
• Scenarios in sourcing comparators clinical supplies
- China as case study
•Approachestomaintainingflexibilitywhilematchingsupply
and demand
• Challenges involved in outsourcing comparator drug
sourcing - what are the ways around this?
• Ways to increase speed of supply
Jasmin Hellwig, Senior Comparator Specialist, MSD
16.00 GDP – Stop talking, more action
• How to implement GDP and work with key stakeholders to
ensure a compliant and secure supply chain
• Case study (Implementing a global GDP complaint QMS for
a 3PL provider
• Developing good relationships and a collaborative
approach to compliance
Amy Shortman, CEO, ASC Associates
16.40 Chairman’s Closing Remarks and Close of Day One
Register online at www.pharmaceutical-logistics.com
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Pharmaceutical Logistics www.pharmaceutical-logistics.com Day Two | Tuesday 19th May 2017
08.30 Registration & Coffee
09.00 Chairman’s Opening RemarksBob Hayes, Director, Seer Pharma
STRATEGIES TO MAINTAIN SUPPLY CHAIN SECURITY, VISIBILITY AND ANTI-COUNTERFEITING
OPENING ADDRESS09.10 An approach to global supply chain security in the
pharmaceutical industry• How a pharmaceutical company with a global supply
chain designs and manages its security system to mitigate
the risk of physical damage, diversion, temperature
excursion, bribery and corruption
• Using internal and external networks as well as technology
the presentation highlights the need for a multi-layered
approach
• Demonstrate case studies where incidents occurred
and what the corrective actions were to mitigate
re-occurrences. This will include looking at investigations
such as paper trails, CCTV footage and forensic analysis to
identify the root cause of the incident
• Supply chain routes by road air and sea Tom Cochrane, Head of Security Operations, Mundipharma
09.50 GS1 standards – a critical tool in the fight against counterfeiting• Standards as a tool to prevent counterfeiting
• Regulatory bodies taking action
• Authentication or traceability – Europe & the world
Glen Hodgson, Head of healthcare, GS1
10.30 Morning Coffee
11.00 The impact of the Falsified Medicines Directive to the supply chain •FalsifiedMedicinesDirective&DelegatedRegulation
•DevelopmentofEuropeanMedicinesVerificationSystems
• The cost implications for the operators
• Status of national implementation and latest developments
Martin FitzGerald, Deputy Director General, European Healthcare Distribution Association (GIRP)
11.40 How TAPA mitigates supply chain security risks•Identification&evaluationofsupplychainRisks
• Intelligence analysis
• Mitigation measures for facilities and transportation
• Collaborative approaches
Jason Breakwell, Vice Chairman, Transported Asset Protection Association (TAPA)
12.20 Networking Lunch
REGULATORY CONSIDERATIONS
13.30 Developing Time and temperature controlled supply chain
risk strategies for emerging markets: Dedicated to Eurasia and
Middle East
• What makes emerging markets different?
•Whatarethespecificchallenges?Byregion
•WhathasbeenSanofiGenzyme’sapproach?
•HowhasSanofiGenzymemitigatedtherisk(s)?
• What can you do to mitigate your risks?
Chris Wallace, Senior Director International Supply Chain,
Sanofi Genzyme
14.10 Risk Management – Back to Basics
• The regulatory requirement for risk-based approach to GDP
compliance
•Whymanagingriskefficientlyandeffectivelyisgoodfor
business
• Industry trends – FMEA, the preferred methodology
• An FMEA model that works!
Bob Hayes, Director, Seer Pharma
14.50 Afternoon Tea
15.20 Maintaining control and managing supplies to the patients
• Control of movement of supplies to depots and study sites
• Global Shipment Integration
• Monitoring trends in shipping lanes
• Personal experiences of visiting a study site
Details to be confirmed
16.00 Temperature mapping in the Ambient Environment
• Requirements and guidance.
• Types of ambient areas to be mapped; static and mobile
• Temperature logger placement; rationale and practical
applications
•Realexamplegraphprofiles
• The control measures used
Chris Bell, Director, TEDAC
16.40 Chairman’s closing remarks and close of day two
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PHARMACEUTICAL LOGISTICS Conference: 18th - 19th May 2017, Copthorne Tara Hotel, Kensington, London, UK
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