Examples of using This active substance in English and their translations into German
{-}
-
Colloquial
-
Official
-
Ecclesiastic
-
Medicine
-
Financial
-
Ecclesiastic
-
Political
-
Computer
-
Programming
-
Official/political
-
Political
This active substance, which has excellent anti-inflammatory properties.
Patent expired in this product 2000 and today there is a multitude of products for agricultural andgardening incorporating this active substance.
This active substance“inhibits the absorption of sugar from the intestine and also the formation of glucose in the liver”.
Pharmacokinetic parameters observed for piperaquine in humans indicate that this active substance has a large volume of distribution 730 l/kg; CV 37.5.
This active substance is absorbed by cells of the thyroid gland(including damage), providing a therapeutic effect.
All notifiers informed the Commission and the rapporteur Member State that they nolonger wished to participate in the programme of work for this active substance.
This active substance is an antiretroviral or antiviral medicine which is used to treat HIV or HBV infection or both.
The applicant informed the Commission and the rapporteur Member State that it nolonger wished to participate in the programme of work for this active substance.
The properties of Jojoba oil, whether against ageing or high temperature,predestine this active substance for use with textiles because even the great stresses involved in the production process do not cause any deterioration.
Proposal for a Council decision concern ing the non-inclusion of aldicarb in Annex 1 to Council Directive 91/414/EEC andthe with drawal of authorisations for plant protection products containing this active substance.
The studies that I have read demonstrated that this active substance has a molecule similar to that of sugar, but it is more coarse which causes it to bind to the intestinal receptor, used for absorption, reversibly blocking it.
The Commission organised two tripartite meetings with the main data submitter andthe rapporteur Member State for this active substance on 18 April 1997 and 11 February 2003.
All notifiers for this active substance informed the Commission and the rapporteur Member State that they no longer wished to participate in the programme of work for this active substance, and therefore further information will not be submitted.
Sera are medicinal products within the meaning of Section 2 sub-section 1 which contain antibodies, fragmentsof antibodies or fusion proteins with a functional antibody component as their active substance and are used because of this active substance.
It is therefore appropriate to include this active substances in Annex I, in order to ensure that in all Member States theauthorisations of plant protection products containing this active substance can be granted in accordance with the provisions of that Directive.
It is therefore appropriate to include these active substances in Annex I, in order to ensure that in all Member States theauthorisations of plant protection products containing this active substance can be granted in accordance with the provisions of that Directive.
Co-administration of umeclidinium bromide with other long-acting muscarinic antagonists ormedicinal products containing this active substance has not been studied and is not recommended as it may potentiate known inhaled muscarinic antagonist adverse reactions.
Whereas it has to be considered that the data required for re-evaluation of this substance will not be submitted in the framework of the work programme and that therefore a decision should be taken with the effect that currentauthorizations for plant protection products containing this active substance are withdrawn;
It is recalled that the initial proposal for a Decision concerned the non-inclusion of aldicarb in Annex I to Council Directive 91/414/EEC andthe withdrawal of authorisations for plant protection products containing this active substance within a period of six months with a period of grace not longer than eighteen months.
Whereas therefore it has to be considered that the data required reevaluation of this substance will not be submitted in the framework of the work programme and that therefore an evaluation of this substance is not possible in this framework; whereas consequently a decision should be taken with the effect that currentauthorizations for plant protection products containing this active substance are withdrawn;
The Council reached agreement on the Decision concerning the non-inclusion of aldicarb in Annex I to Council Directive 91/414/EEC andthe withdrawal of authorisations for plant protection products containing this active substance, on the basis of a Presidency compromise, which the Commission endorsed.
Whereas it has to be considered that a complete data package required for the evaluation of this substance will not be submitted in the framework of the work programme; whereas an evaluation and inclusion in Annex I of this substance is not possible in this framework; whereas consequently a decision should be takenwith the effect that current authorisations for plant protection products containing this active substance are withdrawn;
COMMISSION DECISION of 17 February 1999 concerning the non-inclusion of DNOC of active substance in Annex I to Council Directive 91/414/EEC andthe withdrawal of authorisations for plant protection products containing this active substance(notified under document number C(1999) 332)(Text with EEA relevance) 1999/164/EC.
Thus when a new use of it is proposed, Member States are required to establish a new national provisional MRL in accordance with Article 4(1)(f) of Directive 91/414/EEC before such a newuse of a plant protection product containing this active substance may be authorised.
Where no Community MRL or provisional MRL exists, Member States are to establish a national provisional MRL in accordance with Article 4(1)(f)of Directive 91/414/EEC before plant protection products containing this active substance may be authorised.
In accordance with the provisions of Article 6(3) of the Directive the Commission confirmed in its Decision 98/242/EC(3) that the dossier submitted for azafenidin could be considered as satisfying, in principle, the data and information requirements of Annex II andfor a plant protection product containing this active substance, of Annex III to the Directive.
In accordance with the provisions of Article 6(3) of the Directive Commission Decision 97/164/EC(3) concluded that the dossier submitted for flupyrsulfuron-methyl could be considered as satisfying, in principle, the data and information requirements of Annex II,and for a plant protection product containing this active substance, of Annex III to the Directive.