2017-2018 / Master

Industrial pharmacy

60 crédits

Cycle view

  • Bloc
  • Organisation
  • Théorie
  • Pratique
  • Autres
  • Crédits

Compulsory courses

B1
60Cr
CodeDétailsBlocOrganisationThéoriePratiqueAutresCrédits
PHIN2004-1Active substancesB1TA6
Substances issues de recherches pharmacochimiques, part a   10-- 
Substances issues de recherches pharmacochimiques, part b
Françoise Dufrasne
  5-- 
Substances issues des biotechnologies
David Vermijlen
  15-- 
Substances d'origine naturelle, part a
Joëlle Quetin-Leclercq
  5-- 
Substances d'origine naturelle, part b
Pierre Duez
  5-- 
Produits radiopharmaceutiques
Ghanem Ghanem
  10-- 
PHIN2008-2Clinical viewpointsB1Q16
Métabolisme des médicaments et paramètres pharmacocinétiques
François-Xavier Mathy
  20-- 
Aspects théoriques et pratiques des études cliniques (y compris les méthodes statistiques appliquées aux études cliniques)   15-- 
Information et pharmacovigilance   10-- 
PHIN2013-2Quality assurance and pharmaceutical management B17
Principles of pharmaceutical management   10-- 
Quality assurance, part a : basic concepts and quality assurance organisation
Thierry Pronce
  20-- 
Quality assurance, part b : Analytical technology of procedures and risk analysis
Xavier Marcelis
  7,5-- 
English applied to the pharmaceutical industry
Jacques Poupaert, Nevin Serbest
  20-- 
Pharmaceutical marketing
Vincent Bierlaire
  7,5-- 
PHIN2033-1Industrial pharmaceutical technologyB18
Industrial pharmaceutical microbiology
Véronique Fontaine
  15-- 
Preformulation and selection of galenical forms
Karim Amighi
  15-- 
Industrial production of galenical forms   15-- 
Industrial production of biomolecules
Rita Van Bever
  15-- 
Industrial aspects of technological development including packaging   10-- 
PHIN2023-1Drug analysisB17
Analytical methods and pharmaceutical and biopharmaceutical control, part a
Jean-Michel Kauffman, Pierre Van Antwerpen
  10-- 
Analytical methods and pharmaceutical and biopharmaceutical control, part b   10-- 
Methods in pharmaceutical and biopharmaceutical analysis, part a : Validation and qualification of equipment   15-- 
Methods in pharmaceutical and biopharmaceutical analysis, part b : Process analytical technology   5-- 
Statistical methods applied to the pharmaceutical industry
Laure Elens
  15-- 
Experimental planning and "quality by design"   10-- 
PHIN2029-2Regulation and the medical-social environmentB18
Economic aspects of drug development
Dominique Martin
  10-- 
Legislation and procedures applied to pharmaceutical industry, part a : legislation
Catherine Druez
  105- 
Legislation and procedures applied to pharmaceutical industry, part b : patents and protection
Patrick Di Stefano
  5-- 
Macroeconomic environment and pharmaco-economics
Pierre Duez
  10-- 
CTD File (Common Technical Document)
Jean-Antoine De Muylder
  15-- 
Regulations of preclinical and clinical studies, part a : pharmaceutical toxicological files
Sonia Beken
  15-- 
Regulations of preclinical and clinical studies, part b : clinical studies
Anne Lenaers
  5-- 
Regulations of preclinical and clinical studies, part c : pediatric studies
Daniel Brasseur
  2,5-- 
Specific regulatory issues, part a : medicine and herbal dietary supplement   5-- 
Specific regulatory issues, part b : Preformulation and galenical development documentation
Francis Vanderbist
  5-- 
PHIN2032-1Visits and seminars organised in the pharmaceutical industry - [77,5h Visit]
Françoise Dufrasne, Marianne Fillet, Rita Van Bever
B1--[+]3
MTFE2000-1Final work B1---15