2023-2024 / PHIN2008-2

Clinical viewpoints

Metabolising medication and pharmacokinetic limits

Theoretical and practical views on clinical studies (including the statistical methods applied to clinical studies)

Information and adverse drug events monitoring

Duration

Metabolising medication and pharmacokinetic limits : 20h Th
Theoretical and practical views on clinical studies (including the statistical methods applied to clinical studies) : 15h Th
Information and adverse drug events monitoring : 10h Th

Number of credits

 Advanced Master in Industrial Pharmacy5 crédits 

Lecturer

Metabolising medication and pharmacokinetic limits : François-Xavier Mathy
Theoretical and practical views on clinical studies (including the statistical methods applied to clinical studies) : Régis Radermecker
Information and adverse drug events monitoring : Raphaël Denooz

Coordinator

Philippe Hubert

Language(s) of instruction

French language

Organisation and examination

All year long, with partial in January

Schedule

Schedule online

Units courses prerequisite and corequisite

Prerequisite or corequisite units are presented within each program

Learning unit contents

Theoretical and practical views on clinical studies (including the statistical methods applied to clinical studies)

Methodology of clinical trials

Information and adverse drug events monitoring

This course is dedicated to some notions of Information and Publicity in the field of therapeutic drugs. Pharmacovigilancy aspects are also approached. (Definition and imputability criteria of adverse drugs effects, CBPH operating, ...)

Learning outcomes of the learning unit

Information and adverse drug events monitoring

Table of contents:
1. Pharmacovigilancy: Evaluation of the therapeutic risk
2. Pharmacovigilancy in Belgium and in Europe
3. Information and Publicity
4. Excercices

Prerequisite knowledge and skills

Information and adverse drug events monitoring

Toxicology course of the second cycle

Planned learning activities and teaching methods

Information and adverse drug events monitoring

Pointless

Mode of delivery (face to face, distance learning, hybrid learning)

Information and adverse drug events monitoring

3 courses of 3 or 4 hours
Face to face ou distancial

Recommended or required readings

Information and adverse drug events monitoring

PowerPoint slides

Information and adverse drug events monitoring

Written evalation in january

Work placement(s)

Organisational remarks and main changes to the course

Contacts

Information and adverse drug events monitoring

Pr Raphaël DENOOZ

Clinical and Forensic Toxicological laboratory

CHU B35

Sart-Tilman, B4000 Liège

Tél.04/3237683

Fax 04/3238889

e-mail : Raphael.Denooz@chuliege.be

Association of one or more MOOCs