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“The US based Centre for Medicines in the Public Interest
predicts that counterfeit drug sales will reach US$ 75 billion globally in 2010,
an increase of more than 90% from 2005.” –WHO
Dear Colleague,
Counterfeit pharmaceuticals are an increasing public health
threat and everyone from the pharmaceutical producers, throughout the supply
chain, down to the consumers, will benefit from a coordinated fight against
the fakes. To keep the public safe, new legislation and regulations are imposed,
new technology is developed and the forms for importing and selling
pharmaceuticals are widely debated. With this variety of technologies to choose
from, and so many different legislative changes to obey by, an interchange of
ideas and experiences is vital to every one involved, in the process of getting
safe medicines from the manufacturer to the patients. Further, the understanding
of the complexity of widely debated subjects such as, parallel trade and
internet pharmacies is central to the process of protecting the public.
In the interest of creating an arena for involved companies and
organizations, 3rd Annual Anti Counterfeiting Strategies conference
will focus on:
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The legislative development in Europe and the US
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Technical solutions such as RFID and barcode technology
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International collaboration to combat counterfeiting
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The role of parallel trade and internet pharmacies
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I look forward to seeing you at the conference
Who will be there:
VPs Directors, Heads, and Managers from:
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Pharmaceutical manufacturing and distributing companies
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Wholesalers
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Pharmaceutical packaging and labeling companies
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Anti-counterfeiting technology suppliers
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Anti-counterfeiting service suppliers
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Public health and regulatory bodies
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Anti-counterfeiting organizations
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Non-governmental healthcare organizations
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Pharmaceutical organizations
Key Speakers :-
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Andrew Jackson, Deputy Global Head, Corporate Security,
Novartis
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Monika Dereque-Pois, Secretary General, GIRP
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Sara Dayman, Asset Investigation and Confi scation, BDO Stoy
Hayward
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Jim Thomson, CEO, Centre for Mental Health
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Heinz Kobelt, Secretary General, European Association
Euro-Pharmaceutical Companies
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Janice Kite, Project Manager Traceability in Healthcare, GS1
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Phil Lewis, UK Patent Office
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Tassilo Korab, Executive Director, Health Compliance
Packaging Council
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Christopher Stothers, Associate, Intellectual Property Practice
Group, Milbank, Tweed, Hadley and McCloy
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Eric Noehrenberg, Director, International Trade & Market Policy, International Federation of Pharmaceutical Manufacturers Associations
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Paul Forster-Jones, Managing Director, Cordia Healthcare
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Day
1, Tuesday 1st July 2008
09:30 Registration and
refreshments
10:00 Opening address from the
chair
Eric Noehrenberg
Director,
International Trade & Market Policy
International Federation of
Pharmaceutical Manufacturers Associations
10:10 A global strategy to
fight counterfeiting
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A safe and secure supply chain
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Authentication and traceability
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Activities of regulatory bodies and
industry worldwide
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Global standards – how do they help
fighting counterfeiting?
Janice Kite
Project Manager
Traceability in Healthcare
GS1
10:50 Combating counterfeits of
medicinal products
Tassilo Korab
Executive Director
Health Compliance Packaging
Council
11:30 Morning refreshments
11:50 The costs of counterfeit
drugs
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The burden on the health care
system
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Financial damage due to loss of
sales and a reduced return on R&D investments
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The cost of a damaged brand
Paul Forster-Jones
Managing Director,
Cordia Healthcare
Board Member, UniChem
12:30 Technological and
non-technological measures - How can we protect patients?
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Product coding and identifications
as pre-requisite for tracking and tracing
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Bar codes versus RFID
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EU versus US: are the approaches
different?
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Stake holder and government
initiatives
Monika Dereque-Pois
Secretary General
GIRP
13:10 Networking lunch
14:30 The changes in European
policy
Philip Stevens
Director, Health Program
International
Policy Network*
15:10 The UK national IP crime
strategy
Phil Lewis
UK Patent Office
15:50 Afternoon refreshments
16:10 Anti-Counterfeiting Trading
Agreement
Ilias Konteas
Adviser, Legal
Affairs Department
Businesseurope*
16:50 Panel
discussion: Fighting the fakes – To choose a combat strategy
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Should we focus on
technology, legislation or a logistic approach?
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Will tracking and
tracing keep the supply chain safe?
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Are the various
efforts to combat counterfeiters coordinated enough?
17:40 Closing remarks from the
chair
17:45 Networking drinks
Take your discussions further and build new relationships in a relaxed and
informal setting.
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Day
2, Wednesday 2nd July 2008
09:30 Registration and
refreshments
10:00 Opening address from the
chair
Eric Noehrenberg
Director,
International Trade & Market Policy
International Federation of
Pharmaceutical Manufacturers Associations
10:10 Defending brands & pursuing
offenders: The identification, pursuit, management & recovery of the proceeds of
counterfeiting
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Deterrents & disruption
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Exploration of existing legislative
provision to recover the proceeds of counterfeiting
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Alternative civil remedies
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Global asset tracing:
identification of conduct & property
Sara Dayman
Asset Investigation
and Confiscation
BDO Stoy Hayward
10:50 Analyses for detection of
counterfeit medicines
Christine Eckers
Analytical Sciences
GlaxoSmithKline*
11:30 Morning refreshments
11:50 Experience with RFID and 2D
barcodes
Mark Roberti
Founder and Editor
RFID Journal*
12:30 The importance of packaging
in securing the supply chain
13:10 Networking lunch
14:30 Counterfeit drugs on the
internet
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The relevance of consumer education
as a part of the strategy to fight counterfeit drugs
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Advertising on the internet
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Monitor internet pharmacies
arranging supply chains against counterfeits and diversion through on-line
purchases
Andrew Jackson
Deputy Global Head,
Corporate Security
Novartis
15:10 The reality of internet
pharmacies
Jim Thomson
CEO
Centre for Mental Health
15:50 Afternoon refreshments
16:10 Parallel trade and
counterfeit pharmaceuticals
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The current framework for parallel
trade and repackaging of pharmaceuticals
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Discovery of counterfeit
pharmaceuticals in the parallel supply chain
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Actual and proposed changes to the
distribution and parallel trade framework
Christopher Stothers
Associate,
Intellectual Property Practice Group
Milbank, Tweed, Hadley and
McCloy
16:50 The contribution of parallel
trade distribution to a safe supply chain
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While legal in the EU/EEA area, PT
is often perceived by manufacturers (although not by regulators) as a
weakening of the distribution chain
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The EAEPC argues that its members
provide identical medicines at lower cost than manufacturers’ prices to
patients and final payers. Members share with manufacturers the objective of
fighting against counterfeits and raising the barriers to keep these out of
the legitimate supply chain
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This presentation looks at the
regulatory environment for parallel distribution and looks at the rigorously
controlled business practices of re-packaging/re-labelling, and will
demonstrate the safety profile of the industry. The presentation will address
ways to improve the supply chain without jeopardizing the freedom of movement
of pharmaceutical goods across Europe.
Heinz Kobelt
Secretary General
European Association
Euro-Pharmaceutical Companies
17:30 Chair’s closing remarks
17:40 End of conference
Fee Per Delegate :
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