EMA to have debate on the use of epidemiology in the assessment of drug effects.
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The European Medicines Agency is organising a public debate on the use of epidemiology in the assessment of drug effects at the International Conference on Pharmacoepidemiology & Therapeutic Risk Management congress in Brighton on 20 August 2010. The debate will be moderated by Hans-Georg Eichler, the Agency’s Senior Medical Officer. The Executive Director of the European Medicines Agency, Thomas Lönngren, will deliver the keynote address at ICPE on the same day. Participation is free to attendees of the ICPE congress.
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Damien Bové is THE Drug Development and Regulatory Consultant (pharmaceutical or biotechnology), I work with my clients to define a drug development target, define a drug development strategy, define a regulatory strategy or define a commercial strategy. Our clients are generally raising funds or looking to license out their technology and we help them achieve it. If you want to know more don’t hesitate to get in touch.
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Sign up for the most value add free newsource you can get for free. We spend a huge amount of time and effort monitoring the main drug / device regulators websites for changes in the regulatory environment, and capture between 20 and 40 new regulations, rules and initiatives each month, and summaries them in a fantastic FREE monthly Regulatory and Market Round Up. You can Un-Subscribe at any time and we don not share your details with anybody. You can’t afford to miss out on this service. Just fill in the form below.
“Please note that the pages on this website are designed to provide you with general information only. We make no warranties, representations or undertakings about any of its content. This includes the completeness, accuracy and fitness for any particular purpose, or the content of any third party site referred to or accessed through it. You are personally responsible for ensuring that the information is correct and we will not be held liable or accountable for any mistakes that occur.”
