Traduction de «limits » (Néerlandais → Français) :

TERMINOLOGIE

limited systemische sclerose
sclérose systémique limitée

self-limiting auto-immune thyreoïditis met transiënte hyperthyreoïdie en/of hypothyreoïdie
thyroïdite auto-immune auto-limitante avec hyperthyroïdie transitoire et/ou hypothyroïdie

TRADUCTIONS EN CONTEXTE

COLLECTIF, « Etats limites ou états sans limites ? », Bulletin freudien, Bruxelles, 1997, 29.
BERTRAND M., « L’implication de l’observateur dans l’observation », in L’observation, quels enjeux pour le sujet ?, Buc, Buc Ressource, 2002.

Opmerking 2: er kon geen rekening worden gehouden met opsplitsing tussen grijze garnalen en andere “shrimps” Limit voor shrimps = 2000 (werd gebruikt in de berekening) Limit voor cragnon = 6000
Remarque 2: on n’a pas pu tenir compte de la distinction entre crevettes grises et autres « shrimps » Limit pour shrimps = 2.000 (utilisée dans le calcul) Limit pour cragnon = 6.000

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

For phase I studies, and therefore the large majority of early phase trials, the statutory time limit amounts to just 15 days.
For phase I studies, and therefore the large majority of early phase trials, the statutory time limit amounts to just 15 days.

It is abundantly clear that it is strategically advisable to limit the selection to 3 sub-domains in the start-up phase:
It is abundantly clear that it is strategically advisable to limit the selection to 3 sub-domains in the start-up phase:

Often in the early phases the available quantity of the product is relatively limited.
Often in the early phases the available quantity of the product is relatively limited.

Of the submitted applications, 95% were processed within the set time limits.
Of the submitted applications, 95% were processed within the set time limits.

ESW: één-seconde waarde FVC: geforceerde vitale capaciteit MMMF: Man-Made Mineral Fibres MMVF: Man-Made Vitreous Fibres TEM: transmissie-elektronenmicroscopie TWA: Time Weighted Average (tijd-gewogen-gemiddelde blootstelling) TLV: Threshold Limit Values
AES: alkaline earth silicates CVF : capacité vitale forcée FCR : fibres céramiques réfractaires FVS : Fibres Vitreuses Synthétiques MMVF : Man-Made Vitreous Fibres TWA : Time Weighted Average (exposition moyenne pondérée par le temps) TLV : Threshold Limit Values VEMS : volume expiré en une seconde

Adviesbrief demande NAREDI modifications limites maximales vitamines et minéraux dan les compléments alimentaires (HGR 8905) (enkel in het Frans beschikbaar)
Lettre d'avis - Demande NAREDI modifications limites maximales vitamines et minéraux dans les compléments alimentaires (CSS 8905)

This is related to the entry into force of the royal decree of 14 December 2006, which requires the submission of a PSUR every three years compared with the limitation to just one RQ.
This is related to the entry into force of the royal decree of 14 December 2006, which requires the submission of a PSUR every three years compared with the limitation to just one RQ.