Examples of using An application for authorisation in English and their translations into Swedish
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in a given Member State, an application for authorisation of a clinical trial.
To ensure the reliable functioning of the assessment procedure, however, an application for authorisation of a clinical trial should be withdrawn only for the entire clinical trial.
This Annex outlines the information that may be addressed by those submitting a socioeconomic analysis(SEA) with an application for authorisation, as specified in Article 62(5)(a),
An application for authorisation has been submitted for isopropyl ester of the hydroxylated analogue of methionine which belongs to the group"analogues of aminoacids" referred to in the Annex to Directive 82/471/EEC.
the consignee shall submit an application for authorisation to the competent authorities of that Member State.
CSDs that intend to establish links shall submit an application for authorisation to the competent authority of the requesting CSD as required under point(e) of Article 19(1)
To submit an application for authorisation of genetically modified food
to arrange for such a shipment to be carried out shall submit an application for authorisation to the competent authorities of the country of origin.
shall adopt all necessary measures to comply with this Directive and shall submit an application for authorisation within one year of the deadline for the transposition of this Directive.
within seven years after the entry into force of the Regulation(for additives authorised without a time limit), an application for authorisation will be submitted.
by means of a data-processing technique using the normal procedure to constitute an application for authorisation, provided that.
shall not apply to reference medicinal products for which an application for authorisation has been submitted before the date referred to in Article 90, second paragraph.
Amendments Nos 4 and 5 are also unacceptable because they give undue preference to copy products by granting them authorisation to be placed into circulation even before an application for authorisation has been submitted.
you must submit an application for authorisation to the European Chemicals Agency(ECHA).
can only be carried out after an application for authorisation has been made and determined.
You can apply for authorisation of a biocidal product that is identical to one that has already been authorised following the EU Biocidal Products Regulation, or for which an application for authorisation has been submitted.
the withdrawal of an application, an application for authorisation to any intended Member State concerned.
Only the legal form of a Regulation ensures that the Member States base their assessment of an application for authorisation of a clinical trial on identical criteria, rather than on diverging national transposition measures.
An application for authorisation was submitted for the additive"manganomanganic oxide" as a source of manganese,