Traduction de «committee for medicinal » (Néerlandais → Français) :

Law of 20 July 2006 on the establishment and functioning of the Federal Agency for Medicines and Health Products Royal decrees of 25 February 2007 on the composition and working method of the committees of the Federal Agency for Medicines and Health Products Royal decree of 20 December 2007 determining the date of establishment of the Scientific Committee, namely 1 February 2008 Royal decree of 28 January 2008 on the concrete composition of the Consultative Committee Ministerial decree of 11 January 2007 on the composition and appointment of the members of the executive board of the Federal Agency for Medicines and Health Products
Law of 20 July 2006 on the establishment and functioning of the Federal Agency for Medicines and Health Products Royal decrees of 25 February 2007 on the composition and working method of the committees of the Federal Agency for Medicines and Health Products Royal decree of 20 December 2007 determining the date of establishment of the Scientific Committee, namely 1 February 2008 Royal decree of 28 January 2008 on the concrete composition of the Consultative Committee Ministerial decree of 11 January 2007 on the composition and appointment of the members of the executive board of the Federal Agency for Medicines and Health Products

Consultation platform with FAVV - AFSCA, FPS Public Health and Public Health Minister’s Office DGO - SCM guidance committee (with APB and OPHACO) e-MED (electronic prescription of medicines) (with FPS Public Health and RIZIV - INAMI) “Grey area” consultation platform (with FPS Public Health and FAVV - AFSCA) Guidance committee of the network of medicalpharmaceutical committees ICVV – CICSA Influenza (in cooperation with external partners) Interdepartmental committee of experts on blood, organs, cells, tissues and embryos (with FPS Public Health, KCE, RIZIV - INAMI and WIV - ISP) Inter DG drugs (with FPS Public Health) Mdeon board of management Potassium iodide tablets campaign (with FPS Interior Affairs) Provincial medical commissions (with FPS Public Health) Strategic unit/RIZIV – INAMI Unavailability of medicines (with RIZIV - INAMI)
Consultation platform with FAVV - AFSCA, FPS Public Health and Public Health Minister’s Office DGO - SCM guidance committee (with APB and OPHACO) e-MED (electronic prescription of medicines) (with FPS Public Health and RIZIV - INAMI) “Grey area” consultation platform (with FPS Public Health and FAVV - AFSCA) Guidance committee of the network of medicalpharmaceutical committees ICVV – CICSA Influenza (in cooperation with external partners) Interdepartmental committee of experts on blood, organs, cells, tissues and embryos (with FPS Public Health, KCE, RIZIV - INAMI and WIV - ISP) Inter DG drugs (with FPS Public Health) Mdeon board of management Potassium iodide tablets campaign (with FPS Interior Affairs) Provincial medical commissions (with FPS Public Health) Strategic unit/RIZIV – INAMI Unavailability of medicines (with RIZIV - INAMI)

BAPCOC (with FPS Public Health) Consultation platform with FAVV - AFSCA, FPS Public Health and Public Health Minister’s Office e-MED (electronic prescription of medicines) (with FPS Public Health and RIZIV - INAMI) “Grey area” consultation platform (with FPS Public Health and FAVV - AFSCA) Guidance committee of the network of medicalpharmaceutical committees Interdepartmental committee of experts on blood, organs, cells, tissues and embryos (with FPS Public Health, KCE, RIZIV - INAMI and WIV - ISP) Interdepartmental network on “information society services” (with FPS Economy) Strategic unit/RIZIV – INAMI Unavailability of medicines (with RIZIV - INAMI) Working group on blood of the Belgian Federal Supreme Health Council Working group on cells, tissues and organs of the Belgian Federal Supreme Health Council
BAPCOC (with FPS Public Health) Consultation platform with FAVV - AFSCA, FPS Public Health and Public Health Minister’s Office e-MED (electronic prescription of medicines) (with FPS Public Health and RIZIV - INAMI) “Grey area” consultation platform (with FPS Public Health and FAVV - AFSCA) Guidance committee of the network of medicalpharmaceutical committees Interdepartmental committee of experts on blood, organs, cells, tissues and embryos (with FPS Public Health, KCE, RIZIV - INAMI and WIV - ISP) Interdepartmental network on “information society services” (with FPS Economy) Strategic unit/RIZIV – INAMI Unavailability of medicines (with RIZIV - INAMI) Working group on blood of the Belgian Federal Supreme Health Council Working group on cells, tissues and organs of the Belgian Federal Supreme Health Council

De gegevens over de veiligheid van aliskiren werden recent herbekeken door het Committee for Medicinal Products for Human Use (CHMP) van het European Medicines Agency (EMA) [ www.ema.europa.eu/docs/en_GB/document_library/Medicine_QA/2012/02/WC500122916.pdf ].
Les données concernant le profil d’innocuité de l’aliskirène ont été récemment revues par le Committee for Medicinal Products for Human Use (CHMP) de l’Agence européenne des médicaments (EMA) [ www.ema.europa.eu/docs/en_GB/document_library/Medicine_QA/2012/02/ WC500122916.pdf ].

De werkgroep is per definitie een meer uitgebreide transversale, interdisciplinaire groep en is samengesteld uit de leden van het projectteam plus leden van Committee for Medicinal Products for Human Use (CHMP), Committee for Advanced Therapies (CAT), Paediatric Committee (PDCO) (inclusief voorzitter), PharmacoVigilance Working Party (PhVWP), Scientific Advice Working Party (SAWP) en Co-ordination Group for Mutual Recognition and Decentralised Procedure, human (CMDh).
Le groupe de travail est par définition un groupe interdisciplinaire et transversal plus large, et se compose des membres de l’équipe de projet plus des membres du Committee for Medicinal Products for Human Use (CHMP), Committee for Advanced Therapies (CAT), Paediatric Committee (PDCO) (y compris le président), PharmacoVigilance Working Party (PhVWP), Scientific Advice Working Party (SAWP) et du Co-ordination Group for Mutual Recognition and Decentralised Procedure, human (CMDh).

The law of 20 July 2006 on the establishment and functioning of the FAMHP provides for the creation of a Transparency Committee, a Consultative Committee and a Scientific Committee as advisory bodies to the medicines agency.
The law of 20 July 2006 on the establishment and functioning of the FAMHP provides for the creation of a Transparency Committee, a Consultative Committee and a Scientific Committee as advisory bodies to the medicines agency.

Naar aanleiding van deze gegevens kreeg het Committee for Proprietary Medicinal Products (CPMP), het wetenschappelijk adviesorgaan van het European Agency for the Evaluation of Medicinal Products, de opdracht de baten-risicoverhouding van de hierboven vermelde anorexigenen opnieuw te evalueren.
Prenant en compte ces données, le Comité des Spécialités Pharmaceutiques (CSP), l’organe scientifique de l' Agence Européenne pour l’évaluation des Médicaments, a été chargé de procéder à une réévaluation de la balance bénéfice/risque des anorexigènes mentionnés ci-dessus.

Via zijn afgevaardigden binnen de werkgroep voor de evaluatie van immunologische producten (Immunologicals Working Party - IWP) en binnen het Comité voor geneesmiddelen voor diergeneeskundig gebruik (Committee for Medicinal Products for Veterinary Use – CVMP) heeft het FAGG significant bijgedragen aan het uitwerken van 3 belangrijke documenten over vaccins voor diergeneeskundig gebruik.
Via zijn afgevaardigden binnen de werkgroep voor de evaluatie van immunologische producten (Immunologicals Working Party - IWP) en binnen het Comité voor geneesmiddelen voor diergeneeskundig gebruik (Committee for Medicinal Products for Veterinary Use – CVMP) heeft het FAGG significant bijgedragen aan het uitwerken van 3 belangrijke documenten over vaccins voor diergeneeskundig gebruik.

Sedert 2004 werkt het Europese Herbal Medicinal Product Committee, één van de commissies van het EMA, aan monografieën over planten.
Depuis 2004, le Herbal Medicinal Product Committee européen, l’une des commissions de l’EMA, travaille à la réalisation de monographies sur les plantes.

Deze regelgeving bepaalt wat geneesmiddelen voor innoverende therapie zijn, legt de regels voor de vergunning en controle ervan vast en beschrijft de oprichting van een nieuw comité binnen het Europees bureau voor geneesmiddelen (European Medicines Agency - EMA): het Committee for Advanced Therapies (CAT).
Deze regelgeving bepaalt wat geneesmiddelen voor innoverende therapie zijn, legt de regels voor de vergunning en controle ervan vast en beschrijft de oprichting van een nieuw comité binnen het Europees bureau voor geneesmiddelen (European Medicines Agency - EMA): het Committee for Advanced Therapies (CAT).