Traduction de «entry en medic-e » (Néerlandais → Français) :

TERMINOLOGIE

re-entry ventriculaire-aritmie
Arythmie ventriculaire de réentrée

Omschrijving: De betrokkene wendt bij herhaling symptomen voor zonder duidelijke reden en kan zelfs zichzelf letsel toebrengen teneinde symptomen te veroorzaken. De drijfveren zijn duister en waarschijnlijk verbonden met het oogmerk de rol van zieke aan te nemen. De stoornis gaat dikwijls samen met opvallende stoornissen van de persoonlijkheid en in relaties. | Neventerm: | Münchhausen-syndroom | medical shopping
Définition: Simulation répétée de symptômes, sans objectifs évidents, avec parfois auto-mutilation dans le but de provoquer des signes ou des symptômes. Les motifs ne sont pas clairs, et probablement internes, visant à obtenir un rôle de malade et s'accompagnent souvent d'une perturbation nette de la personnalité et des relations. | Hospitalisme Patient itinérant Syndrome de Münchhausen

TRADUCTIONS EN CONTEXTE

medicines for human use and veterinary medicines, raw materials (active ingredients) for pharmacists, establishment of retail pharmacies, medical devices) ●● Management of possible crisis situations ●● Coordination of the (inter)national representation of the FAMHP ●● The difference between the roles of “Communication” versus “Information” ●● Points of entry for applications submitted to
medicines for human use and veterinary medicines, raw materials (active ingredients) for pharmacists, establishment of retail pharmacies, medical devices) ●● Management of possible crisis situations ●● Coordination of the (inter)national representation of the FAMHP ●● The difference between the roles of “Communication” versus “Information” ●● Points of entry for applications submitted to

c) heeft elke gemachtigd gebruiker die ofwel over een gebruikersnaam, een paswoord en een burgertoken ofwel over een elektronische identiteitskaart beschikt toegang tot de toepassingen ”Elektronische gegevensuitwisseling voor het Vlaams Agentschap Zorg & Gezondheid (VESTA)”, “Kankerregistratie”, “Technische Cel via het web (eTCT)”, “Elektronische geboorteaangifte (eBirth)”, “BelRAI”, “Raadplegen van de verzekerbaarheid van een persoon”, “Doorsturen van facturen derde betaler”, “eBox Update Info”, “Project on Cancer of the Rectum, online applicatie voor de registratie van rectumkanker (PROCARE DATA ENTRY)” en “Medic-e intern - Elektronische invoer en raadpleging van de evaluatie van de personen met een handicap”;
c) chaque utilisateur habilité qui dispose soit d’un Identifiant, d’un Mot de Passe et d’un Token de citoyen, soit d’une Carte d’Identité Electronique, a accès aux applications « Système électronique d’échange de données pour la Vlaams Agentschap voor Zorg & Gezondheid (VESTA) », « Enregistrement du cancer », « Cellule technique via le web (eTCT) », « Notification électronique de naissance (eBirth) », « BelRAI »,

Toegang tot PROCARE data entry
Accéder à PROCARE data entry

This is related to the entry into force of the royal decree of 14 December 2006, which requires the submission of a PSUR every three years compared with the limitation to just one RQ.
This is related to the entry into force of the royal decree of 14 December 2006, which requires the submission of a PSUR every three years compared with the limitation to just one RQ.

Meer informatie over PROCARE data entry
Plus d'information sur PROCARE data entry

Klinisch onderzoek wordt verricht in overeenstemming met de Verklaring van Helsinki, vastgesteld door de 18e World Medical Assembly in Helsinki, Finland, 1964, en gewijzigd door de 29e World Medical Assembly in Tokio, Japan, 1975, en door de 35e World Medical Assembly in Venetië, Italië, 1983.
mondiale à Helsinki, Finlande, et modifiée en 1975 par la vingt-neuvième assemblée médicale mondiale à Tokyo, Japon, ainsi qu'en 1983 par la trente-cinquième assemblée médicale mondiale à Venise, Italie.

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

Medical devices The European medical devices directives are socalled New Approach Directives: the products can be commercialised without the involvement of the competent authorities.
Medical devices The European medical devices directives are socalled New Approach Directives: the products can be commercialised without the involvement of the competent authorities.

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
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

At European level, important texts were adopted such as Directive 2007/47/EC amending Directive 93/42/EEC concerning medical devices and Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, and Regulation (EC) no. 1394/2007 on advanced therapy medicinal products.
At European level, important texts were adopted such as Directive 2007/47/EC amending Directive 93/42/EEC concerning medical devices and Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, and Regulation (EC) no. 1394/2007 on advanced therapy medicinal products.