Traduction de «useful to warn its » (Néerlandais → Français) :

Nearer to us, a Belgian university thinks it useful to warn its students both against the abuse of beverages that suppress fatigue without eliminating the need for rest and against mixing them with alcohol (De Duve, 2009).
Plus près de chez nous, une université belge juge utile de mettre en garde ses étudiants contre la consommation abusive de ces boissons qui masquent la fatigue sans supprimer le besoin de repos ainsi que vis-à-vis de l’association avec l’alcool (De Duve, 2009).

- the warning signs of depressive and/or suicidal behaviour;
o les symptômes d’alerte d’un comportement dépressif et / ou suicidaire;

It enables the various parties involved to perceive the warning signs, to know what to do when these situations occur.
Elle permet aux divers intervenants de détecter des signes annonciateurs, de savoir comment agir lorsque ces situations se présentent.

Recognising high-risk individuals and situations at an early stage: identifying certain (explicit, ambiguous or implicit) warning signs, having environmental factors under control, examining the indicator for the evolution of the suicidal thoughts provide real means for preventing suicide.
L’identification précoce des sujets et situations à risque: la reconnaissance de certains signes (explicites, ambigus ou implicites), le contrôle des facteurs environnementaux, l’exploration de l’indicateur d’évolution de l’idée suicidaire autorisent de réelles possibilités de prévention.

Warning limit: + 2 standard deviations
Limite d'avertissement : + 2 écarts types

besmette personen afkomstig zijn van een geografisch sterk verspreid gebied, moet een " early warning system" tussen de Belgische deelgebieden worden voorzien, dat in actie treedt wanneer een vermoeden bestaat van een epidemische uitbraak van Legionellose.
potentiellement contaminées proviennent de régions géographiquement très dispersées, un " early warning system" doit être prévu entre les différentes parties du territoire belge, qui entre en action lorsqu'on présume qu’une épidémie de Légionellose pourrait se déclarer.

After investigation, these complaints and other spontaneous checks gave rise to the issue of 11 formal charges and 27 warnings
After investigation, these complaints and other spontaneous checks gave rise to the issue of 11 formal charges and 27 warnings

Het lijkt de Hoge Gezondheidsraad aangewezen dat dit " early warning system" zowel voor de binnenlandse als de buitenlandse activering op het federaal niveau zou worden gecoördineerd.
Le Conseil Supérieur d'Hygiène considère comme indiqué que ce " early warning system" soit coordonné au niveau fédéral, tant pour ses activités à l’intérieur du pays que vis-à-vis de l’étranger.

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