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Traduction de «report a medicines » (Néerlandais → Français) :

1974 on the opening, transfer and merger of retail pharmacies Royal decree of 9 July 1984 on the provision of information and advertising relating to medicines Royal decree of 11 January 1993 determining the conditions under which medicines for human use may be supplied in sample form Royal decree of 7 April 1995 on the provision of information and advertising relating to medicines for human use Royal decree of 15 July 1997 on active implantable medical devices, transposing Directive 90/385 EEC (AIMD) Royal decree of 19 December 1997 on the control and analysis of the raw materials used by dispensing chemists Royal decree of 18 March 199 ...[+++]

1974 on the opening, transfer and merger of retail pharmacies Royal decree of 9 July 1984 on the provision of information and advertising relating to medicines Royal decree of 11 January 1993 determining the conditions under which medicines for human use may be supplied in sample form Royal decree of 7 April 1995 on the provision of information and advertising relating to medicines for human use Royal decree of 15 July 1997 on active implantable medical devices, transposing Directive 90/385 EEC (AIMD) Royal decree of 19 December 1997 on the control and analysis of the raw materials used by dispensing chemists Royal decree of 18 March 199 ...[+++]


In this first “annual report”, we have chosen to describe the transition from the DG Medicinal Products of the FPS Public Health to an autonomous medicines agency and provide more details about a number of activities in 2007.

In this first “annual report”, we have chosen to describe the transition from the DG Medicinal Products of the FPS Public Health to an autonomous medicines agency and provide more details about a number of activities in 2007.


Healthcare professionals and consumers of medicines and health products need to be made aware of the utility and obligation (in the case of materiovigilance and haemovigilance) of reporting adverse effects and adverse events associated with the use of medicines and health products to the FAMHP. Furthermore, the report form should be made easy to complete

Healthcare professionals and consumers of medicines and health products need to be made aware of the utility and obligation (in the case of materiovigilance and haemovigilance) of reporting adverse effects and adverse events associated with the use of medicines and health products to the FAMHP. Furthermore, the report form should be made easy to complete


European Commission, High level group on innovation and provision of medicines, recommendations for action., 7 May 2002, G10 medicines report. [http ...]

European Commission, High level group on innovation and provision of medicines, recommendations for action. 7 May 2002, G10 medicines report. [http ...]


ema.europa.eu/Find medicine/Human medicines/European Public Assessment Reports. Lees de

L’EPAR complet relatif à Soliris est disponible sur le site web de l’Agence, sous: : ema.europa.eu/Find


Zie voor het volledige EPAR voor Evoltra de website van het Agentschap onder ema.europa.eu/Find medicine/Human medicines/European Public Assessment Reports. Lees de bijsluiter (ook onderdeel van

ema.europa.eu/Find medicine/Human medicines/European Public Assessment Reports. Pour plus


At the end of 2007 the FAMHP initiated a programme for specific monitoring of new medicines (“black triangle” – symbol included in the BCFI-CBIP annotated drugs formulary – Gecommentarieerd Geneesmiddelenrepertorium – Répertoire Commenté des Médicaments) with the aim of encouraging healthcare professionals to report adverse effects of medicines with a new active substance to the FAMHP.

At the end of 2007 the FAMHP initiated a programme for specific monitoring of new medicines (“black triangle” – symbol included in the BCFI-CBIP annotated drugs formulary – Gecommentarieerd Geneesmiddelenrepertorium – Répertoire Commenté des Médicaments) with the aim of encouraging healthcare professionals to report adverse effects of medicines with a new active substance to the FAMHP.


This report exists in Dutch, French and English The electronic version of this annual report 2007 is available on the FAMHP’s website www.fagg.be - www.afmps.be / Medicines / FAGG

This report exists in Dutch, French and English The electronic version of this annual report 2007 is available on the FAMHP’s website www.fagg.be - www.afmps.be / Medicines / FAGG


This report “The Federal Agency for Medicines and Health Products – 2008 in words and images. Annual Report 2008” was created under the coordination of the Communication Division of the FAMHP.

This report “The Federal Agency for Medicines and Health Products – 2008 in words and images. Annual Report 2008” was created under the coordination of the Communication Division of the FAMHP.


A MEDICINES AGENCY UNDER CONSTRUCTION Annual report 2007

A MEDICINES AGENCY UNDER CONSTRUCTION Annual report 2007




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Date index: 2024-10-14
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