Traduction de «veterinary medicinal » (Néerlandais → Français) :

Veterinary medicines The Veterinary Medicines unit ensures the quality, safety and efficacy of veterinary medicines in the interests of public health and animal welfare. This involves the following set of tasks: ●● Granting MA for veterinary medicines
Veterinary medicines The Veterinary Medicines unit ensures the quality, safety and efficacy of veterinary medicines in the interests of public health and animal welfare. This involves the following set of tasks: ●● Granting MA for veterinary medicines

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 1999 on medical devices, transposing Directive 93/42/EEC of 14 June 1993 (MDD) Royal decree of 11 July 2003 determining the conditions under which medicines for veterinary use may be supplied in sample form Law of 16 December 2004 modifying the regulations on combating abuses in the promotion of medicines Royal decree of 10 June 2006 establishing the report point referred to in Article 10, § 5, of the law of 25 March 1964 on medicines Royal decree of 23 November 2006 implementing Article 10, § 3, of the law of 25 March 1964 on medicines Royal decree of 25 February 2007 recognising the institutions referred to in Article 10 § 3 of the law of 25 March 1964 on medicines
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 1999 on medical devices, transposing Directive 93/42/EEC of 14 June 1993 (MDD) Royal decree of 11 July 2003 determining the conditions under which medicines for veterinary use may be supplied in sample form Law of 16 December 2004 modifying the regulations on combating abuses in the promotion of medicines Royal decree of 10 June 2006 establishing the report point referred to in Article 10, § 5, of the law of 25 March 1964 on medicines Royal decree of 23 November 2006 implementing Article 10, § 3, of the law of 25 March 1964 on medicines Royal decree of 25 February 2007 recognising the institutions referred to in Article 10 § 3 of the law of 25 March 1964 on medicines

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

narcotics and concerning risk limitation and therapeutic advice and of 22 January 1998 governing certain psychotropic substances and concerning risk limitation and therapeutic advice and of 12 April 1974 containing certain provisions relating to substances with hormonal, antihormonal, anabolic, beta-adrenergic, anti-infectious, antiparasitic and anti-inflammatory action Law of 15 July 1985 on the use in animals of substances with hormonal, anti-hormonal, beta-adrenergic or production stimulating action Law of 13 June 1986 on the removal and transplanting of organs, with regard to cells and tissues Law of 28 August 1991 on the practice of veterinary medicine, regarding the provision of medicines to animal carers Law of 5 July 1994 on blood and blood derivatives of human origin Law of 7 May 2004 on experiments on the human person Royal decree of 31 May 1885 approving new instructions for physicians, pharmacists and druggists Royal decree of 22 September 1966 on the conditions and arrangements for the recognition of laboratories for the analysis and checking of medicines Royal decree of 6 June 1960 on the production, preparation and wholesale distribution and delivery of medicines Royal decree no. 78 of 10 November 1967 on the practice of the healthcare professions regarding the dispensing of medicines to the public and Royal decree of 25 September
narcotics and concerning risk limitation and therapeutic advice and of 22 January 1998 governing certain psychotropic substances and concerning risk limitation and therapeutic advice and of 12 April 1974 containing certain provisions relating to substances with hormonal, antihormonal, anabolic, beta-adrenergic, anti-infectious, antiparasitic and anti-inflammatory action Law of 15 July 1985 on the use in animals of substances with hormonal, anti-hormonal, beta-adrenergic or production stimulating action Law of 13 June 1986 on the removal and transplanting of organs, with regard to cells and tissues Law of 28 August 1991 on the practice of veterinary medicine, regarding the provision of medicines to animal carers Law of 5 July 1994 on blood and blood derivatives of human origin Law of 7 May 2004 on experiments on the human person Royal decree of 31 May 1885 approving new instructions for physicians, pharmacists and druggists Royal decree of 22 September 1966 on the conditions and arrangements for the recognition of laboratories for the analysis and checking of medicines Royal decree of 6 June 1960 on the production, preparation and wholesale distribution and delivery of medicines Royal decree no. 78 of 10 November 1967 on the practice of the healthcare professions regarding the dispensing of medicines to the public and Royal decree of 25 September

Veterinary medicines Unit For the fifth year in a row the number of applications closed for obtaining marketing authorisation (MA) within the Veterinary medicines Unit has exceeded the number of new applications submitted.
Veterinary medicines Unit For the fifth year in a row the number of applications closed for obtaining marketing authorisation (MA) within the Veterinary medicines Unit has exceeded the number of new applications submitted.

This KPI does not relate to applications relating to vigilance for veterinary medicines, or to research and development for veterinary medicines.
This KPI does not relate to applications relating to vigilance for veterinary medicines, or to research and development for veterinary medicines.

Some current and future projects of the Veterinary Medicines unit In addition to active participation in numerous projects with an impact on different departments or services or even on the entire organisation, there are also a number of projects specifically for the Veterinary Medicines unit, such as: ●● The computerisation of the databases for
Some current and future projects of the Veterinary Medicines unit In addition to active participation in numerous projects with an impact on different departments or services or even on the entire organisation, there are also a number of projects specifically for the Veterinary Medicines unit, such as: ●● The computerisation of the databases for

Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency.
Règlement (CE) n o 726/2004 du Parlement européen et du Conseil du 31 mars 2004 établissant des procédures communautaires pour l'autorisation et la surveillance en ce qui concerne les médicaments à usage humain et à usage vétérinaire, et instituant une Agence européenne des médicaments, JO L 136 du 30 avril 2004, pp.0001-0033 ( [http ...]

De eenheid Geneesmiddelen voor diergeneeskundig gebruik zal ook nauw samenwerken met het Center for Veterinary Medicines (CVM) van de Amerikaanse Food and Drug Administration en met het Amerikaanse ministerie van Landbouw om praktische regelingen tot stand te brengen in verband met de verdere ontwikkeling van de geheimhoudingsovereenkomsten die eind 2004 tussen de VS en de EU zijn gesloten met het oog op de uitwisseling van informatie en documenten.
L’unité vétérinaire travaillera en étroite collaboration avec le Center for Veterinary Medicines (CVM, Centre des médicaments vétérinaires) de la Food and Drug Administration ainsi qu’avec le ministère fédéral de l’agriculture des États-Unis pour mettre en oeuvre des dispositions pratiques en vue de faire progresser les accords de confidentialité convenus entre les États-Unis et l’UE à la fin 2004 pour l’échange d’informations et de documents.

EMEA/CVMP/413/99-Rev 1 VEDDRA List of clinical terms for reporting adverse reactions in animals to veterinary medicines Wordt herzien op basis van het PhVWP-V-werkprogramma voor 2005 (VEEDRA-subgroep komt op 5 mei 2005 bijeen; wordt op 5 juli 2005 door de PhVWP-V en op 5 september 2005 door het CVMP aangenomen)
EMEA/CVMP/413/99-Rev 1 VEDDRA List of clinical terms for reporting adverse reactions in animals to veterinary medicines À réviser selon le programme de travail du PhVWP-V pour 2005 (réunion du sous-groupe VEDDRA en mai 2005; adoption par le PhVWP en juillet 05 et le par le CVMP en septembre 05)