University of Liege | Version française
	Study programmes 2010-2011 Last update : 11/04/2011
	PHIN2029-1   Regulation and the medical-social environment - Legislation and procedures applied to pharmaceutical industry, part a : legislation - Legislation and procedures applied to pharmaceutical industry, part b : patents and protection - Economic and medical social medicine - CTD File (Common Technical Document) - Regulations of preclinical and clinical studies, part a : pharmaceutical toxicological files - Regulations of preclinical and clinical studies, part b : clinical studies - Regulations of preclinical and clinical studies, part c : pediatric studies - Specific regulatory issues, part a : medicine and herbal dietary supplement - Specific regulatory issues, part a : galenic developement Duration :   Legislation and procedures applied to pharmaceutical industry, part a : legislation : 10h Th, 5h Pr Legislation and procedures applied to pharmaceutical industry, part b : patents and protection : 5h Th Economic and medical social medicine : 10h Th CTD File (Common Technical Document) : 15h Th Regulations of preclinical and clinical studies, part a : pharmaceutical toxicological files : 15h Th Regulations of preclinical and clinical studies, part b : clinical studies : 5h Th Regulations of preclinical and clinical studies, part c : pediatric studies : 2,5h Th Specific regulatory issues, part a : medicine and herbal dietary supplement : 5h Th Specific regulatory issues, part a : galenic developement : 5h Th Credits/ECTS :   Advanced Master in Industrial Pharmacy Toute l'année 7 Holder(s) :   Legislation and procedures applied to pharmaceutical industry, part a : legislation : Catherine Druez Legislation and procedures applied to pharmaceutical industry, part b : patents and protection : Sylvie Ponchaut Economic and medical social medicine : Alain De Wever CTD File (Common Technical Document) : Jean‑Antoine De Muylder Regulations of preclinical and clinical studies, part a : pharmaceutical toxicological files : Sonia Beken Regulations of preclinical and clinical studies, part b : clinical studies : A Lenaers Regulations of preclinical and clinical studies, part c : pediatric studies : Daniel Brasseur Specific regulatory issues, part a : medicine and herbal dietary supplement : Monique Tits Specific regulatory issues, part a : galenic developement : Francis Vanderbist Coordinator :   Philippe Hubert Language :   French language Home Search by Faculty Search by teacher Search by course code and title
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