Vertaling van "for medical devices " (Nederlands → Frans) :

TERMINOLOGIE

neuromyelitis optica [Devic]
Neuromyélite optique [Devic]

IUD - intra-uterien device
dispositif intra-utérin

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

IN-CONTEXT TRANSLATIONS

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

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.

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.

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

Qermid©Coronaire stents - Quality oriented Electronic Registration of Medical Implant Devices
Qermid©Défibrillateurs Cardiaques - Quality oriented Electronic Registration of Medical Implant Devices

Qermid©Hartdefibrillatoren - Quality oriented Electronic Registration of Medical Implant Devices
Qermid©Pacemakers - Quality oriented Electronic Registration of Medical Implant Devices

Qermid©Endoprothesen - Quality oriented Electronic Registration of Medical Implant Devices
Qermid©Endoprotheses - Quality oriented Electronic Registration of Medical Implant Devices

» Toegankelijkheid van het eHealth-platform voor nieuwe doelgroepen » Geïnformeerde toestemming van de patiënt – nota goedgekeurd door het Sectoraal Comité » Een nieuwe toepassing: Qermid©Endoprothesen - Quality oriented Electronic Registration of Medical Implant Devices
» De nouveaux groupes-cibles autorisés à accéder au portail de la plate-forme eHealth » Consentement éclairé du patient, la note est approuvée par le comité sectoriel » Une nouvelle application: Qermid©Endoprotheses - Quality oriented Electronic Registration of Medical Implant Devices

Qermid©Hartdefibrillatoren - Quality oriented Electronic Registration of Medical Implant Devices | eHealth
Qermid©Défibrillateurs Cardiaques - Quality oriented Electronic Registration of Medical Implant Devices | eHealth

Qermid©Coronaire stents - Quality oriented Electronic Registration of Medical Implant Devices | eHealth
Qermid©Tuteurs coronaires - Quality oriented Electronic Registration of Medical Implant Devices | eHealth