Vertaling van "registration applications " (Nederlands → Frans) :

TERMINOLOGIE

extracorporele applicator voor hyperthermiesysteem voor extravasculaire circulatie
applicateur extracorporel de système d’hyperthermie de circulation extravasculaire

applicator voor aneurysmaclip
applicateur de clips d’anévrisme

applicator voor compressiekousen
enfile-bas de contention

applicator voor dermale anesthesie
applicateur dermique d’anesthésie locale

handbediende applicator voor brachytherapiesysteem voor oog
applicateur manuel de système de brachythérapie oculaire

applicator voor thermisch pulsatiesysteem voor ooglid
applicateur pour système de traitement thermique par impulsions sur les paupières

intracorporele applicator voor hyperthermiesysteem voor extravasculaire circulatie
applicateur intracorporel de système d’hyperthermie de circulation extravasculaire

handbediende applicator voor oesofageaal brachytherapiesysteem
applicateur manuel de système de brachythérapie pour l’œsophage

applicator voor oesofageaal brachytherapiesysteem met op afstand bedienbare afterloading
applicateur de système de brachythérapie pour l’œsophage à chargement différé à distance

applicator voor tandheelkundige hars
applicateur de matériau de restauration dentaire

IN-CONTEXT TRANSLATIONS

In 2007 23 CP applications, including 1 new registration, were also started up with Belgium as (co)-rapporteur, and Belgium was RMS for 7 new registration applications via the DCP.
In 2007 23 CP applications, including 1 new registration, were also started up with Belgium as (co)-rapporteur, and Belgium was RMS for 7 new registration applications via the DCP.

Optimisation of the integrated MeSeA system At the time of the FAMHP’s creation, the organisation had just one integrated system, MeSeA, to support its core business, i.e. the electronic submission of registration applications and variations for medicines for human use and the pharmacovigilance applications.
Optimisation of the integrated MeSeA system At the time of the FAMHP’s creation, the organisation had just one integrated system, MeSeA, to support its core business, i.e. the electronic submission of registration applications and variations for medicines for human use and the pharmacovigilance applications.

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

Development in the number of registration applications for medicines for human use
Development in the number of registration applications for medicines for human use

d) heeft elke gemachtigd gebruiker die over een elektronische identiteitskaart beschikt toegang tot de toepassingen “Shared Artritis File for Electronic Use (SAFE)”, “Raadpleging van de wilsverklaring inzake euthanasie - eutha-consult”, “ORTHOpedic Prosthesis Identification Data - Electronic Registry - ORTHOpride®”, “Project on cancer of the rectum - Central Image Repository (PROCARE RX)”, “Qermid(c)Pacemakers-Quality Electronic Registration of Medical Implant Devices”, “SMUREG”, “Medico-Administratieve Stromen – Thuisverpleging (MEDADM-INF)”, “ZNA - Zorgportaal – SARAi”, “Registratie van Therapeutische Projecten (TherPro – PatientRegistration)”, “Medega”, “QermidDefibrilateur-Quality Electronic Registration of Medical Implant Devices”, “eHealthBox”, “QermidEndoprothèses-Quality Electronic Registration of Medical Implant Devices”, “QermidPacemakers-Quality Electronic Registration of Medical Implant Devices”, “QermidTuteurs Coronaires- Quality Electronic Registration of Medical Implant Devices”, “Registratiemodule van de Belgische Virtuele Tumorbank”, “Catalogus van de Belgische Virtuele Tumorbank”, “CIVARS – Chapter IV Agreement Requesting System”, “Web Application Metahub”, “Raadpleging van medische kaart”, “TDI - Registratie Module van de “Treatment Demand Indicator””, “eShop - Online bestelling getuigschriften voor verstrekte hulp (Medattest)”, “BNMDR - Belgian NeuroMuscular Disease Registry”, “eHealthConsent”, “Moduledatabank Jeugdhulp Vlaanderen” en “Authentieke bron geneesmiddelen”.
d) chaque utilisateur habilité qui dispose d’une Carte d’Identité Electronique a accès aux applications « Shared Artritis File for Electronic Use (SAFE) », « Consultation de la déclaration anticipée d’euthanasie- eutha-consult », « ORTHOpedic Prosthesis Identification Data - Electronic Registry - ORTHOpride® », « Project on cancer of the rectum - Central Image Repository (PROCARE RX) », « Qermid(c)Pacemakers- Quality Electronic Registration of Medical Implant Devices », « SMUREG », « Flux Medico-Administratifs - Infirmier A Domicile (MEDADM-INF) », « ZNA - Zorgportaal – SARAi », « Enregistrement des projets thérapeutiques (TherPro – PatientRegistration) », « Medega », « QermidDefibrilateur-Quality Electronic Registration of Medical Implant Devices », « eHealthBox », « QermidEndoprothèses- Quality Electronic Registration of Medical Implant Devices », « QermidPacemakers- Quality Electronic Registration of Medical Implant Devices », « QermidTuteurs Coronaires-Quality Electronic Registration of Medical Implant Devices », « Module d’enregistrement de la Tumorothèque Virtuelle Belge », « Catalogue de la Tumorothèque Virtuelle Belge », « CIVARS – Chapter IV Agreement Requesting System », « Web Application Metahub », « Consultation des cartes médicales », « TDI

Some achievements of the evaluation commission for herbal medicines (plants working group) in 2007 were ●● The monitoring of applications ●● The first applications for TU registration ●● The TU notification project ●● Interaction with the “grey area” consultation
Some achievements of the evaluation commission for herbal medicines (plants working group) in 2007 were ●● The monitoring of applications ●● The first applications for TU registration ●● The TU notification project ●● Interaction with the “grey area” consultation

The Registration (marketing authorisation) department of the FAMHP is responsible for evaluating new applications and applications for changes to existing marketing authorisations (variations), with a view to grant the authorisation for marketing a medicine or health product.
The Registration (marketing authorisation) department of the FAMHP is responsible for evaluating new applications and applications for changes to existing marketing authorisations (variations), with a view to grant the authorisation for marketing a medicine or health product.

Application presentation: Electronic registration and exchange of guard duty data in Flanders (.Powerpoint).
Application presentation: Electronic registration and exchange of guard duty in Flanders (.Powerpoint).

The Registration (marketing authorisation) department for its part is required to evaluate applications for a marketing authorisation (MA), for the sake of the National Procedure (NP), the European Decentralised Procedure (DCP), the Mutual Recognition Procedure (MRP) and the Central Procedure (CP).
The Registration (marketing authorisation) department for its part is required to evaluate applications for a marketing authorisation (MA), for the sake of the National Procedure (NP), the European Decentralised Procedure (DCP), the Mutual Recognition Procedure (MRP) and the Central Procedure (CP).

1. Zoals voorzien in de bestuursovereenkomst, werkt het Rijksinstituut voor Ziekte- en Invaliditeitsverzekering (RIZIV) aan de implementatie van een reeks geautomatiseerde registers met betrekking tot bepaalde implantaten, die gevoed worden door webtoepassingen en « System to System »-diensten (applications Quality oriented Electronic Registration of Medical Implants and invasive Devices – QERMID).
1. Tel que le prévoit son contrat d'administration, l’Institut national d’assurance maladieinvalidité (INAMI) met en œuvre un ensemble de registres automatisés relatifs à la pose de certains implants et alimentés par des applications Web et des services « System to System » (applications Quality oriented Electronic Registration of Medical Implants and invasive Devices – QERMID).