Clinical Trials:ICH GCP training

Clinical Trials:ICH GCP training - Event details   12/17/2008 - 12/18/2008 BRATISLAVA HOTEL, KIEV, Kiev, UKRAINE   Description On behalf of the NBScience Org. it is our honor and pleasure to announce that 8 ICH GCP meeting : "ICH, GCP rules, regulatory (EMEA, FDA) GCP inspections.Key documents." will be held in Kiev, Ukraine. We would like to cordially invite you to participating in this biannual meeting . The major aim of the 8th GCP Meeting is to bring together scientist from all around the world who are mostly focused in their research and studies on ICH GCP, clinical trials. We strongly believe that such a meeting makes for an excellent occasion to exchange and share recent achievements and ideas in this fascinating field of medicine. Hightlights include: - "Main principles of Good Clinical Practice (GCP). Regulatory acts of the European Union and International Conference of Harmonization (ICH). Responsibilities and the rights of the parties participating in clinical trials. Interaction of Sponsor and Investigator. Responsibilities of Investigator, Sponsor according to principles of Good Clinical Practice (GCP)” - "Ethical aspects of clinical trials of medical products. Informed consent .File of Investigator; keeping of documentation.” - Development and the Research Budget - Review of (drug, device, biologics) development program, including protocol development, Case Report Form design, project and program management, assessing costs and building budgets. How to develop budgets and strategies for reducing costs (at the investigational site). And much more! Category Medical Equipment & Technologies Management More details (event webpage):  www.nbscience.com Apply for event:  Link Event language:  English Contact info:  NBScience in Eastern Europe Phone: +38(044) 533-12-70 Fax: +38(063) 277-64-65 Email: oleg.evtushenko.ukraine@nbscience.com Contact form:  Link

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