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BIOTECHNOLOGY EUROPE-BELGIUM EVENTS

   

 

 

 

 

   
 

   
 
   
   
   
   
   
   
   
   
 
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
Pediatric Pharmacology Europe
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.
 

 
2nd Annual Pharmaceutical Market & Patient Access for Chronic Disease Therapies
14th-15th September 2010
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.

 

 
5th Annual Clinical Outsourcing Partnerships In Central & Eastern Europe
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.
 

 
Optimizing Early Phase Oncology Studies to Accelerate Proof of Concept
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.
 

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.
 

Predictive Human Toxicity and ADME/Tox Studies
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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