Vertaling van "may be inferred from " (Nederlands → Frans) :

Resistance to ß-lactams may be inferred from testing only oxacillin.
La résistance aux ß-lactames peut être déduite en testant seulement l'oxacilline.

During one’s lifetime, there may be interference from potential triggering stressors, which may be of a biogenetic, psychological, somatic, or social nature.
Les déclencheurs potentiels de stress, qui peuvent être de nature biogénétique, psychologique, somatique ou social-communautaire, peuvent interférer dans la vie.

Apart from the risks involved in tackling such delicate matters in the media, the latter may also play a very active part in suicide prevention by spreading information within the context of a report on a suicide.
A côté des risques que présente l’abord de questions aussi délicates dans les médias, ceux-ci peuvent aussi jouer un rôle très actif dans la prévention du suicide en publiant des informations dans le cadre d’un reportage sur un suicide.

In doing so, health professionals may also partially prevent the past from having a negative influence on their professional activities when faced with similar requests for help”. 17 ( [http ...]
De cette manière, le professionnel peut également éviter en partie que le passé ait une influence négative sur ses actions médicales lors de nouvelles demandes d’aide similaires.

Finally, the idea “that gloom forms an integral part of old age” may also prevent a depression from being detected in elderly people (or lead to therapeutic nihilism).
Enfin, l’idée “que la morosité fait partie intégrale de la vieillesse” peut également empêcher la détection d’une dépression chez les personnes âgées (ou mener au nihilisme thérapeutique).

2. In case of an outbreak, screening may differentiate " imported cases" , or re-admissions of colonised patients (positive culture within 48 hours after admission) from new cases of nosocomial colonisation or infection (positive culture later than 48 hours after admission).
2. En cas d’éclosion, le dépistage peut différencier les " cas importés" , ou les réadmissions de patients colonisés (culture positive dans un délai de 48 heures après l’admission) de nouveaux cas de colonisation ou d’infection nosocomiale (culture positive ultérieure à 48 heures après l’admission).

The cases dealt with in these meetings may be complaints by consumers or producers, requests for advice from inspection services, formal opinions on the formulation of regulations, formal opinions for companies wishing to market products and to ensure that they are presenting their product correctly, and internal cases that serve for the compilation of guidelines for the consultation platform.
The cases dealt with in these meetings may be complaints by consumers or producers, requests for advice from inspection services, formal opinions on the formulation of regulations, formal opinions for companies wishing to market products and to ensure that they are presenting their product correctly, and internal cases that serve for the compilation of guidelines for the consultation platform.

It may formulate advice about any matters relating to the policies being followed or to be pursued by the FAMHP. This committee consists of representatives of patients and users, of all sectors who are involved in the matters under the Agency’s mission, as well as representatives from the relevant federal public services.
It may formulate advice about any matters relating to the policies being followed or to be pursued by the FAMHP. This committee consists of representatives of patients and users, of all sectors who are involved in the matters under the Agency’s mission, as well as representatives from the relevant federal public services.

The law of 7 May 2004 relating to experiments on the human person in Belgium provides that any objections from the FAMHP need to be submitted within a maximum of 28 days following the validation of applications for clinical trials.
The law of 7 May 2004 relating to experiments on the human person in Belgium provides that any objections from the FAMHP need to be submitted within a maximum of 28 days following the validation of applications for clinical trials.

The EFSA notes that it may turn out to be necessary to collect data on the real exposure that results from consuming energy drinks, especially for teenagers and young adults.
L’EFSA constate qu’il pourrait s’avérer nécessaire de recueillir des données concernant l’exposition réelle due à la consommation de boissons « énergisantes », notamment pour les adolescents et les jeunes adultes.