Vertaling van "référant " (Nederlands → Frans) :

The FAMHP wants: ●● To emerge as a point of reference for scientific advice ●● To attract clinical trials ●● To act as rapporteur or RMS in the evaluation of registration applications for important products ●● Where relevant, to be a point of reference
The FAMHP wants: ●● To emerge as a point of reference for scientific advice ●● To attract clinical trials ●● To act as rapporteur or RMS in the evaluation of registration applications for important products ●● Where relevant, to be a point of reference

1. Deze machtigingsaanvraag werd ingediend door het Centre communautaire de référence pour le dépistage des cancers (hierna “CCR” of “Centre de référence” genoemd), een vereniging zonder winstoogmerk met als opdracht de coördinatie en de evaluatie van de programma’s voor de opsporing van kanker (borstkanker en colorectale kanker) in de Franse Gemeenschap en de Duitstalige Gemeenschap.
1. La présente demande d’autorisation est introduite par le Centre communautaire de référence pour le dépistage des cancers (dénommé ci-après « CCR » ou « Centre de référence »), une association sans but lucratif ayant pour but la coordination et l'évaluation des programmes de dépistage des cancers (du sein et colorectal) en Communauté française et en Communauté germanophone.

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 1999 on medical devices, transposing Directive 93/42/EEC of 14 June 1993 (MDD) Royal decree of 11 July 2003 determining the conditions under which medicines for veterinary use may be supplied in sample form Law of 16 December 2004 modifying the regulations on combating abuses in the promotion of medicines Royal decree of 10 June 2006 establishing the report point referred to in Article 10, § 5, of the law of 25 March 1964 on medicines Royal decree of 23 November 2006 implementing Article 10, § 3, of the law of 25 March 1964 on medicines Royal decree of 25 February 2007 recognising the institutions referred to in Article 10 § 3 of the law of 25 March 1964 on medicines
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 1999 on medical devices, transposing Directive 93/42/EEC of 14 June 1993 (MDD) Royal decree of 11 July 2003 determining the conditions under which medicines for veterinary use may be supplied in sample form Law of 16 December 2004 modifying the regulations on combating abuses in the promotion of medicines Royal decree of 10 June 2006 establishing the report point referred to in Article 10, § 5, of the law of 25 March 1964 on medicines Royal decree of 23 November 2006 implementing Article 10, § 3, of the law of 25 March 1964 on medicines Royal decree of 25 February 2007 recognising the institutions referred to in Article 10 § 3 of the law of 25 March 1964 on medicines

The European directives regarding medical devices are referred to as the New Approach Directives. Products may be commercialised without the intervention of a competent authority.
The European directives regarding medical devices are referred to as the New Approach Directives. Products may be commercialised without the intervention of a competent authority.

Verdunningen " Reference dossier dilution" (PDF, 151.82 Kb)
Dilutions " Reference dossier dilution" (PDF, 151.82 Kb)

In order to regulate the quality and relevance of messages to the public, a prior licence is required for radio and TV information campaigns about human health and illness which refer directly or indirectly to medicines. This licence is normally issued by the Minister responsible following advice from the Commission for the supervision of advertising for medicines for human use.
In order to regulate the quality and relevance of messages to the public, a prior licence is required for radio and TV information campaigns about human health and illness which refer directly or indirectly to medicines. This licence is normally issued by the Minister responsible following advice from the Commission for the supervision of advertising for medicines for human use.

It is also clear that the number of submitted applications continues to rise sharply compared with previous reference periods.
It is also clear that the number of submitted applications continues to rise sharply compared with previous reference periods.

BERAADSLAGING NR 11/063 VAN 20 SEPTEMBER 2011 MET BETREKKING TOT DE VERWERKING VAN PERSOONSGEGEVENS TUSSEN HET CENTRE COMMUNAUTAIRE DE RÉFÉRENCE POUR LE DÉPISTAGE DES CANCERS EN DE STICHTING KANKERREGISTER IN HET KADER VAN DE EVALUATIE VAN DE PROGRAMMA’S VOOR DE OPSPORING VAN BORSTKANKER EN COLORECTALE KANKER
DÉLIBÉRATION N° 11/063 DU 20 SEPTEMBRE 2011 RELATIVE AU TRAITEMENT DE DONNÉES À CARACTÈRE PERSONNEL ENTRE LE CENTRE COMMUNAUTAIRE DE RÉFÉRENCE POUR LE DÉPISTAGE DES CANCERS ET LA FONDATION REGISTRE DU CANCER DANS LE CADRE DE L’ÉVALUATION DES PROGRAMMES DE DÉPISTAGE DU CANCER DU SEIN ET DU CANCER COLORECTAL

Beraadslaging nr 11/063 van 20 september 2011 met betrekking Tot de verwerking van persoonsgegevens tussen het centre Communautaire de référence pour le dépistage des cancers en De stichting kankerregister in het kader van de evaluatie van De programma’s voor de opsporing van borstkanker en Colorectale kanker.
Délibération n° 11/063 du 20 septembre 2011 relative au traitement de données à caractère personnel entre le centre communautaire de référence pour le dépistage des cancers et la fondation registre du cancer dans le cadre de l’évaluation des programmes de dépistage du cancer du sein et du cancer colorectal.

To check the quality and relevance of the messages conveyed to the public, a preliminary check was introduced in 2007 for radio/ TV information campaigns about human health and human diseases that refer directly or indirectly to medicines
To check the quality and relevance of the messages conveyed to the public, a preliminary check was introduced in 2007 for radio/ TV information campaigns about human health and human diseases that refer directly or indirectly to medicines