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De Well Established Use-procedure;

Vertaling van "use and establishing " (Nederlands → Frans) :

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 199 ...[+++]

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 199 ...[+++]


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 h ...[+++]

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 h ...[+++]


Herbal medicinal products In line with the provisions of the royal decree of 14 December 2006, three procedures are used for the issue of the MA or registration for herbal medicinal products: the full procedure, the “Well Established Use” procedure and a third specific procedure for traditional herbal medicines as stipulated in article 43 of the royal decree.

Herbal medicinal products In line with the provisions of the royal decree of 14 December 2006, three procedures are used for the issue of the MA or registration for herbal medicinal products: the full procedure, the “Well Established Use” procedure and a third specific procedure for traditional herbal medicines as stipulated in article 43 of the royal decree.


Zowel voor well established use als voor traditional use werken fabrikanten volgens de " Good Manufacturing Practice " (GMP).

Que ce soit pour le well established use ou le traditional use , les fabricants procèdent selon les bonnes pratiques de fabrication (Good Manufacturing Practices ou GMP).


Zowel voor well established use als voor traditional use werken fabrikanten volgens de “Good Manufacturing Practice” (GMP).

Que ce soit pour le well established use ou le traditional use, les fabricants procèdent selon les bonnes pratiques de fabrication (Good Manufacturing Practices ou GMP).


Conform de bepalingen van het koninklijk besluit (K.B) van 14 december 2006 bestaan er drie procedures om een VHB of registratie toe te kennen voor kruidengeneesmiddelen: de volledige procedure, de “Well Established Use”- procedure en een derde, specifieke procedure voor traditionele kruidengeneesmiddelen zoals bedoeld in artikel 43 van dat besluit.

Conformément aux dispositions de l’arrêté royal (A.R) du 14 décembre 2006, il existe trois procédures d’application pour accorder l’AMM ou l’enregistrement des médicaments à base de plantes : la procédure complète, la procédure « Well Established Use » et une troisième procédure spécifique pour les médicaments traditionnels à base de plantes telle que visée à l’article 43 de cet arrêté.


A vaccines for veterinary use project team was established to support the daily activities of the spearhead in line with the defined strategic objectives.

A vaccines for veterinary use project team was established to support the daily activities of the spearhead in line with the defined strategic objectives.


In addition to the daily activities (inspections, granting of licences/authorisations/certificates, RAS) the Production & Distribution Department also focused efforts in 2008 on gradually solving the backlog of Dutch language establishment applications and transfer applications for retail pharmacies. Additionally, the backlog in respect of raw materials used by retail pharmacies was also tackled.

In addition to the daily activities (inspections, granting of licences/authorisations/certificates, RAS) the Production & Distribution Department also focused efforts in 2008 on gradually solving the backlog of Dutch language establishment applications and transfer applications for retail pharmacies. Additionally, the backlog in respect of raw materials used by retail pharmacies was also tackled.


Voor well established use moeten de actieve bestanddelen minstens 10 jaar beschikbaar zijn als geregistreerd geneesmiddel in minstens één land van de Europese Unie.

Pour le well established use , les principes actifs doivent être disponibles comme médicament enregistré depuis au moins 10 ans dans au moins un pays de l’Union européenne.






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Date index: 2021-11-09
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