Traduction de «medicines as stipulated in article » (Néerlandais → Français) :

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.

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

Que l'article 767, § 2, alinéa 1er, du Code judiciaire stipule que si l'avis est donné par écrit, le Ministère public en donne lecture et le dépose à l'audience dans le délai fixé par le juge conformément à l'article 766, alinéa, 1er, aux jour et heure fixés lors de la clôture des débats et indiqués sur la feuille d'audience; que l'avis est déposé toutefois dans le même délai au greffe sans qu'il en soit fait lecture lorsque le premier juge en a décidé ainsi ou dans le cas visé à l'article 755; que l'article 767, § 2, alinéa 2, précise que lorsque l'avis ne peut être rendu dans le délai, la cause du retard est indiquée sur la feuille d'audience;
Que l’article 767, § 2, alinéa 1er, du Code judiciaire stipule que si l’avis est donné par écrit, le Ministère public en donne lecture et le dépose à l’audience dans le délai fixé par le juge conformément à l’article 766, alinéa, 1er, aux jour et heure fixés lors de la clôture des débats et indiqués sur la feuille d’audience; que l’avis est déposé toutefois dans le même délai au greffe sans qu’il en soit fait lecture lorsque le premier juge en a décidé ainsi ou dans le cas visé à l’article 755; que l’article 767, § 2, alinéa 2, précise que lorsque l’avis ne peut être rendu dans le délai, la cause du retard est indiquée sur la feuille d’audience;

This article stipulates The regulation states that production, quality and pharmacovigilance standards need to be determined for these products;
This article stipulates The regulation states that production, quality and pharmacovigilance standards need to be determined for these products;

Applications for already notified homeopathic medicines will have to be submitted in line with a timetable which will be set by the Minister of Public Health in accordance with article 14 of the royal decree of 23 June 1999.
Applications for already notified homeopathic medicines will have to be submitted in line with a timetable which will be set by the Minister of Public Health in accordance with article 14 of the royal decree of 23 June 1999.

Mdeon follows the guidelines authorised in connection with its recognition and ensures strict compliance with the legal requirements (article 10 of the law of 25 March 1964 on medicines).
Mdeon follows the guidelines authorised in connection with its recognition and ensures strict compliance with the legal requirements (article 10 of the law of 25 March 1964 on medicines).

In an article published in the journal for Evidence Based Medicine Minerva (February 2006) G. Pieters, a Belgian specialist on the subject, looks into this possibility: “SSRI’s worden beschouwd als effectief en veilig voor de behandeling van tal van aandoeningen.
Dans un article de la revue d’evidence based medicine Minerva (février 2006), un spécialiste belge analyse cette éventualité: « Les ISRS sont considérés comme efficaces et sûrs dans le traitement de plusieurs affections.