The
importance of the Asia Pacific region as a clinical
trials hub continues to increase significantly. Latest
reports indicate that more than 90% of clinical trials
conducted in Asia are multinational in scope with
South Korea, India, Taiwan and China being the most
popular in terms of trials launched by the top 20
global pharmaceutical companies.
Patient access and market access are viewed as
significant reasons for conducting clinical trials in
Asia, however different countries within the reason as
seen as providing variable benefits. For example
whilst China is seen as the leader in being able to
recruit large volumes of patients at a reasonable low
cost, Japan is perceived as providing the highest
quality data for trials. Elsewhere approval times in
South Korea and Singapore are significantly lower than
most other Asia Pacific countries.
In general, global pharmaceutical companies’
headquarters still tend to lead the operations of
global and multinational clinical trials remotely in
all Asian countries except for Japan but this trend is
changing as more pharmaceutical companies strive to
establish a regional presence.
The past five years has seen more than half of the
multinational pharmaceutical companies forming
strategic partnerships with CROs in Asia and further
partnerships have also been initiated with local CROs
or through global CROs subcontracting with local CROs
who are playing an increasing important role.
So what does the
future hold for the Asia Pacific region and it’s
role in conducting clinical trials?
The 2nd Asia Clinical Trials Outsourcing Congress will
take an in depth view of the regions increasing
importance and examine where this trend will lead as
well as reviewing strategic and operational
implications and regulatory and logistical obstacles
and barriers.
Presentations, panel debates and round table
discussions will include the following topics –
Benchmarking
best practices to establish a solid clinical
trials strategy in Asia
Pacific
Its not
all about cost! Analysing other key factors
influencing conducting clinical trials in Asia
Establishing
relationship with local CROs and their changing
role in the clinical trial process
Utilising
Asia Pacific as hub for multi-national clinical
trials
Data
collection and management challenges in Asia
Pacific
Overview
of new regulatory requirements in India
The
rise of Korea as a centre for conducting clinical
trials
–
clinical trial case study
Commercialisation
opportunities in Asia Pacific
What
progress has been made in IP protection in Asia
Pacific
Assessing
the strong physician-patient relationships created
in different Asian countries and how these can
increase enrolment and retention
Safety
monitoring and risk management of clinical trials
in Asia
Establishing
a solid supply chain strategy for clinical trials
in Asia
Country
specific case study analysis
2011 Sponsors
For
further information please contact;
Steve Hambrook Conference Director
steve@globalengage.co.uk
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