Traduction de «for the notification and supervision » (Néerlandais → Français) :

The FAMHP is also the competent authority for the notification and supervision of the notified bodies based in Belgian territory.
The FAMHP is also the competent authority for the notification and supervision of the notified bodies based in Belgian territory.

checked prior to publication. Radio and television advertisements are provided with a licence after advice from the Commission for the supervision of advertising of medicines for human use or after notification to the FAMHP for the other media.
checked prior to publication. Radio and television advertisements are provided with a licence after advice from the Commission for the supervision of advertising of medicines for human use or after notification to the FAMHP for the other media.

Meldingsplicht Een vaststelling van een besmetting moet gemeld worden aan uw provinciale controle-eenheid van het FAVV. Voor adressen en verdere informatie over meldingsplicht, zie de website: [http ...]
Notification obligatoire La découverte d’une contamination doit être notifiée à l’unité provinciale de contrôle de l’AFSCA. Adresses et autres informations sur la notification obligatoire, voir site web : [http ...]

Each application for such licences is accompanied by an extensive investigation of the legitimacy of the application and of the market participants 280 Pre export notifications (PEN) 1224 preliminary notifications of intra-Community transactions
Each application for such licences is accompanied by an extensive investigation of the legitimacy of the application and of the market participants 280 Pre export notifications (PEN) 1224 preliminary notifications of intra-Community transactions

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.

The main difference from the DG Medicinal Products is the FAMHP’s more autonomous way of working under the supervision and responsibility of the Minister of Public Health.
The main difference from the DG Medicinal Products is the FAMHP’s more autonomous way of working under the supervision and responsibility of the Minister of Public Health.

The main difference from the DG Medicinal Products is that the FAMHP can function more autonomously under the supervision and responsibility of the Minister of Public Health.
The main difference from the DG Medicinal Products is that the FAMHP can function more autonomously under the supervision and responsibility of the Minister of Public Health.

Advisory commission which is consulted e.g. in cases of non-availability of medicines Commission for the approval of institutions assigning preliminary approvals for scientific events Commission for the establishment of retail pharmacies and chambers of appeal (Frenchspeaking chamber and Dutch-speaking chamber) Commission for the recognition of pharmacists-clinical biologists Commission for the supervision of advertising for medicines for human use Evaluation commission for active implantable medical devices Evaluation commission for homeopathic medicines Evaluation commission for medical devices Evaluation commission for medicines for human use Evaluation commission for medicines for veterinary use Evaluation commission for traditional herbal medicines Pharmacopoeia commission
Advisory commission which is consulted e.g. in cases of non-availability of medicines Commission for the approval of institutions assigning preliminary approvals for scientific events Commission for the establishment of retail pharmacies and chambers of appeal (Frenchspeaking chamber and Dutch-speaking chamber) Commission for the recognition of pharmacists-clinical biologists Commission for the supervision of advertising for medicines for human use Evaluation commission for active implantable medical devices Evaluation commission for homeopathic medicines Evaluation commission for medical devices Evaluation commission for medicines for human use Evaluation commission for medicines for veterinary use Evaluation commission for traditional herbal medicines Pharmacopoeia commission

PCE Luxemburg Rue du Vicinal 1 – 2 de verdieping, 6800 Libramont T 061/21 00 60 – F 061/21 00 79 info.LUX@afsca.be notif.LUX@afsca.be
UPC Luxembourg Rue du Vicinal 1 – 2 ème étage, 6800 Libramont T 061/21 00 60 – F 061/21 00 79 Info.LUX@afsca.be notif.LUX@afsca.be

Hij moet de hierboven vermelde maatregelen toepassen maar zal er ook voor kunnen opteren om alle andere alternatieve bestrijdingsmaatregelen die later door het Agentschap goedgekeurd zouden kunnen worden toe te passen. Hij dient het gevarenregister de datum van vaststelling, de identificatie van de percelen, de analyseresultaten en de toegepaste maatregelen te vermeldenDe bepalingen van de meldingsplicht zijn voorts beschreven in het bericht beschikbaar via de volgende link: [http ...]
Il appliquera les mesures citées ci-dessus mais également toute autre mesure de lutte qui pourrait être ultérieurement approuvée par l’Agence et enregistrera au registre des dangers la date de découverte, l’identification des parcelles, les résultats d’analyses et les mesures appliquéesles modalités de notification sont détaillées dans le communiqué accessible via le lien suivant : [http ...]