Examples of using Authorised in the community in English and their translations into Swedish
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Ecclesiastic
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Official/political
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Computer
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Programming
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Political
consistent so that all medicinal products authorised in the Community can be effectively monitored.
has been authorised in the Community.
of any of the regulated entities authorised in the Community or on its own initiative.
Directive 2004/39/EC lays down common regulatory requirements relating to investment firms wherever authorised in the Community, and governing the functioning of regulated markets and other trading systems Official Journal L 145 of 30.4.2004.
Ensuring the dissemination of information on adverse reactions to medicinal products authorised in the Community by means of a database permanently accessible to all Member States;
Ensuring the dissemination of information on adverse reactions to medicinal products authorised in the Community, by means of a database permanently accessible to all Member States;
i.e. one that has not yet been authorised in the Community, and for which the therapeutic indication is the treatment of acquired immune deficiency syndrome,
both when the marketing of such material is authorised in the Community and when this presence is tolerated by virtue of this Regulation.
produced from GMOs both when the marketing of such GMOs is authorised in the Community and when their adventitious
reinsurance undertakings authorised in the Community or on its own initiative.
it is appropriate that MRLs premised on the notion that use of the substance concerned is not authorised in the Community should not apply until the end of the phasing-out period applying to that substance.
of any of the regulated entities authorised in the Community or on its own initiative.
As a result of the detection of residues from the pharmacologically active substance malachite green whose use in veterinary medicinal products for food producing animals is not authorised in the Community, and its metabolite leucomalachite green in aquaculture products, the level to be set for harmonised MRPL for that substance has
An application for marketing authorisation under Article 6 of Directive 2001/83/EC in respect of a medicinal product for human use which is not authorised in the Community at the time of entry into force of this Regulation shall be regarded as valid only if it includes, in addition to the particulars
it is appropriate that MRLs premised on the notion that use of the substance concerned is not authorised in the Community, should not apply until the end of the phasing-out period applying to that substance.
premised on the notion that use of the substance concerned is not authorised in the Community should not apply until the end of the phasing-out period applying to that substance.
containing a new active substance that has not been authorised in the Community by[date] the ten-year period provided for in the first subparagraph of paragraph 1 shall be extended by one year for each extension of the marketing authorisation to another food producing species if it is authorised within the five years following the granting of the initial marketing authorisation.
containing a new active substance that has not been authorised in the Community by[date] the ten-year period provided for in the first subparagraph of paragraph 1 shall be extended by one year for each extension of the marketing authorisation to another food‑producing species,