Safety Monitoring of Medicinal Products: Guidelines for Setting Up and Running a Pharmacovigilance Centre
(2000; 28 pages) [French]
Table des matières
Afficher le documentINTRODUCTION
Afficher le document1. WHY PHARMACOVIGILANCE?
Afficher le document2. DEFINITION AND AIMS
Ouvrir ce répertoire et afficher son contenu3. HOW TO START A PHARMACOVIGILANCE CENTRE
Ouvrir ce répertoire et afficher son contenu4. REPORTING OF ADVERSE DRUG REACTIONS
Ouvrir ce répertoire et afficher son contenu5. SPECIAL ISSUES IN REPORTING
Ouvrir ce répertoire et afficher son contenu6. PRACTICALITIES IN THE ORGANISATION OF A PHARMACOVIGILANCE CENTRE
Ouvrir ce répertoire et afficher son contenu7. ASSESSMENT OF CASE REPORTS
Ouvrir ce répertoire et afficher son contenu8. USE OF THE DATA
Fermer ce répertoire9. RELATIONS WITH OTHER PARTIES
Afficher le document9.1 The Drug Regulatory Authority
Afficher le document9.2 Pharmaceutical companies
Afficher le document9.3 Professional medical and pharmaceutical associations
Afficher le document9.4 World Health Organization
Afficher le document9.5 National pharmacovigilance centres
Afficher le document9.6 Academia
Afficher le document9.7 Media and consumer organisations
Afficher le document10. OTHER SOURCES OF INFORMATION
Afficher le document11. FUNDING
Afficher le documentREFERENCES
Afficher le documentGLOSSARY
Afficher le documentCAUSALITY CATEGORIES
Afficher le documentWHO CONTACTS
 

9.6 Academia

Academia: The need for pharmacovigilance and the nature of its procedures are a natural part of the curriculum of pre-graduate training. In addition a pharmacovigilance centre may contribute to and participate in postgraduate educational programs. Findings or hypotheses from the pharmacovigilance system may be of potential interest for further study with regard to mechanisms, reaction frequency, and so on, to academic pharmacological or epidemiological institutions and departments.

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Dernière mise à jour: le 3 mai 2013