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Pediatric Pharmacology Europe |
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13th-14th
September 2010 |
This will be a
two-day meeting for clinical
pharmacologists, scientists and
pediatricians to discuss overcoming the
scientific challenges using tools such as
models & simulations and PK & PD studies to
optimise the development of new pediatric
medicines.
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2nd Annual Pharmaceutical
Market & Patient Access for Chronic Disease Therapies |
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14th-15th
September 2010 |
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Chronic diseases are taking a steadily
increasing share of national health spending in
the developed world, especially due to an ageing
population and unhealthy lifestyles. Such
conditions and treatments do not often seem as
controversial and as high on the political,
healthcare system and media‘s agenda, when
compared to the very expensive cancer or orphan
drugs, for example. Typically, drugs for chronic
diseases are priced at very reasonable levels,
yet are making a large budget impact, effecting
significant percentages of the entire
population. The total number of patients are
growing from year to year as medicines improve
in efficacy and patients live longer. Health
spending on long-term diseases, is indeed a
long-term problem for payers, who are now
looking to reprioritise budgets in a difficult
economic environment and also allocate more
resources to prevention, earlier diagnosis,
improved managed care, disease management,
reducing wastage through better patient
adherence and investing in one-off surgical
procedures involving medical devices.

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5th Annual Clinical
Outsourcing Partnerships In Central & Eastern Europe |
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27th-28th September-2010 |
Central & Eastern Europe
continues to be a standout region for high quality
clinical research, with its well-trained
investigators and large patient populations. Due to
this popularity the clinical outsourcing environment
in CEE & Russia is becoming more complex and
difficult to navigate. This event will examine the
multitude of outsourcing practices being used in the
region today, as over the past 2-3 years several
powerful yet inherently different outsourcing
cultures have emerged in the region. These Preferred
Provider and Functional Service Provider models have
evolved in the region at varying levels of success
and they both bring with them a multitude of
opportunities and challenges for sponsors and
clinical solution providers alike.
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Optimizing Early Phase
Oncology Studies to Accelerate Proof of Concept |
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29th-30th September-2010 |
When
running early clinical trials for experimental new
drugs across a range of therapeutic areas,
demonstrating "proof of concept" is a critical
milestone of the development process. It is at this
stage where exploratory studies become confirmatory
studies and there is a basis for studying the
efficacy in a larger population. From a business
perspective, showing proof of concept is also an
essential bargaining chip when negotiating licensing
agreements.
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Predictive Human Toxicity and
ADME/Tox Studies - training course
26th
& 27th
January
2011 |
This course is specifically
designed for personnel in the pharmaceutical and
biotechnology industries and contract research
organizations (CROs) who need to understand the
requirements for ADME (absorption, distribution,
metabolism, elimination), pharmacokinetics/toxicokinetics
(PK/TK) and drug metabolism (DM) experiments during
the drug discovery and development processes.
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Predictive
Human Toxicity and ADME/Tox Studies |
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27th
& 28th
January
2011 |
The desire to bring new drugs
to market faster is a key driver of pharmaceutical
companies. Being able to identify drug candidates
faster with fewer missed hits has streamlined the
screening process, but having insufficient knowledge
of potential human toxicity early on can turn a
successful drug into a devastating loss.
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