Primeri uporabe Described in sections v Angleški in njihovi prevodi v Slovenski
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Financial
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Computer
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Official/political
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Programming
Available data are described in sections 4.8, 5.1 and 5.2.
Licensee and Third Party use of such modifications andderivatives is limited to the license rights described in Sections this Agreement.
Available data are described in sections 5.1 and 5.2 but no recommendation on a posology can be made.
Currently available data are described in sections 4.4 and 5.1 but no recommendation on a posology can be made.
Currently available data are described in sections 4.8 and 5.1 but no recommendation on a posology can be made.
Currently available data are described in sections 4.4 and 5.1 but no recommendation on a posology can be made.
When a device is put into service,Member States may require the information described in sections 13, 14 and 15 of Annex 1 to be in their national language(s).
Current available data are described in sections 4.4, 4.8, 5.1 and 5.2 but no recommendation on a posology can be made.
Exporting producers, Union producers, importers andrepresentative associations who made information available in accordance to the procedures described in sections 5.3, 5.4 and 5.5 above will be considered as interested parties if there is an objective link between their activities and the product under investigation.
Currently available data are described in sections 4.8, 5.1, 5.2 and 5.3 but no recommendation on a posology can be made.
Currently available data in adolescents from 12 to 17 years are described in sections 4.8, 5.1 and 5.2, but no recommendation on a posology can be made.
Currently available data are described in sections 4.8 and 5.1. AZOPT is not recommended for usein infants, children and adolescents.
Finally, it is important to note that even where a particularmaterial satisfies the tests set out by the ECJ(and described in sections 3.3) in order to be considered as a non-waste, if it is in practice discarded, it must clearly be considered and treated as a waste.
With the exception of the processing described in Sections 3.2 and 5, we will not forward your personal data to recipients established outside the European Union or the European Economic Area.
Currently available limited data are described in sections 4.8, 5.1, and 5.2 but no recommendation on a posology can be made.
Currently available data are described in sections 4.8, 5.1 and 5.2, but no recommendation on a posology can be made.
Currently available data are described in sections 5.1 and 5.2 but no recommendation on a posology can be made.
Currently available data are described in sections 4.8, 5.1, and 5.2 but no recommendation on a posology can be made.
These effects are described in section 4,‘Possible side effects'.
Signs and symptoms of kidney disease are described in section 4.
Currently available data on paediatric use are described in section 5.1.
Reconstitute the lyophilisate as described in section 6.6. Initial intravenous bolus:.
Details are described in Section 6.2.7.
Available pharmacokinetic data are described in section 5.2.
The procedure for reconstitution is described in section 6.6.