Traduction de «regulations and determining » (Néerlandais → Français) :

TERMINOLOGIE

regulator voor koolstofdioxide-cilinder
régulateur de bouteille de dioxyde de carbone

regulering van menstruatie | ter voorkoming van zwangerschap
Interruption de grossesse Régulation cataméniale

zuurstofcilinder met geïntegreerde regulator
bouteille d’oxygène à régulateur fixe

TRADUCTIONS EN CONTEXTE

The agenda items for the first meeting will include the appointment of the president and vice-president, the drafting and approval of the commission’s rules and regulations and determining the dates of meetings.
The agenda items for the first meeting will include the appointment of the president and vice-president, the drafting and approval of the commission’s rules and regulations and determining the dates of meetings.

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

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;

While each Member State has its own way of governing its health system, ministries of health set the vision for the health development and have the mandate and responsibility for legislation, regulation and enforcement of health policies, as well as for gathering intelligence on health and its social, economic and environmental determinant.
Bien que chaque État membre ait un mode de gouvernance de son système de santé qui lui est propre, ce sont les ministères chargés de la santé qui définissent les perspectives de développement du système de santé et qui ont le mandat et la responsabilité en matière de législation, de réglementation et de mise en œuvre des politiques de la santé, ainsi que pour réunir les connaissances et les analyses sur la santé et ses déterminants sociaux, économiques et environnementaux.

Work is proceeding on adjusting the existing regulations in order to introduce administrative simplifications, such as the accelerated determination of the acceptability of submitted applications.
Work is proceeding on adjusting the existing regulations in order to introduce administrative simplifications, such as the accelerated determination of the acceptability of submitted applications.

The rate of routine inspections is determined by international regulations or recommended by European or national guidelines.
The rate of routine inspections is determined by international regulations or recommended by European or national guidelines.

The seriousness of the situation, the differences in regulations from country to country, the difficulty of determining at the start of an incident whether it is a quality problem or a problem of pharmacovigilance, are factors which have to be taken into account.
The seriousness of the situation, the differences in regulations from country to country, the difficulty of determining at the start of an incident whether it is a quality problem or a problem of pharmacovigilance, are factors which have to be taken into account.