Примери за използване на Applications for authorisation на Английски и техните преводи на Български
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REACH Applications for authorisation.
Adopted opinions andprevious consultations on applications for authorisation.
Subsequent applications for authorisation.
Reporting and exchange of information on applications for authorisation.
Applications for authorisation- current consultations- ECHA.
It would therefore be pointless to allow the submission of applications for authorisation.
Formats for applications for authorisation- ECHA.
The fees for review reports are the same as for applications for authorisation.
All applications for authorisation shall be acknowledged as quickly as possible.
The review report is also submitted within one of the“submission windows” established for applications for authorisation.
Any applications for authorisation needed to exercise his service activities.
IUCLID is the tool used to prepare, for example,REACH registration dossiers and applications for authorisation of biocidal products.
Applications for authorisation may be made by the manufacturer(s), importer(s) and/or downstream user(s) of the substance.
The advice provided by the Authority shallbe without prejudice and non-committal as to the subsequent assessment of applications for authorisation by the Scientific Panels.
Applications for authorisation can cover uses of a given substance by the applicant, uses further down in the supply chain, or both.
Uses of ADCA are very diverse and concern a broad range of different manufacturing industries,expected to lead to highly complex applications for authorisation.
Applications for authorisation are submitted to a Member State, acting as zonal rapporteur, who evaluates the application for the relevant zone.
Restrictions that exist when the substance in question is added to the list of substances for which applications for authorisation can be submitted, should be maintained for that substance.
The applications for authorisation of additives listed in the annexes to this Regulation were submitted before the date of application of Regulation(EC) No 1831/2003.
In the case of biocidal products containing more than one active substance, applications for authorisation shall be submitted no later than the date of approval of the last active substance for that product-type.
Applications for authorisation for replantings referred to in Article 66(1) of Regulation(EU) No 1308/2013 may be submitted at any time during the same wine year in which the grubbing up takes place.
Studies to be performed in order to demonstrate the safety of the GM food and feed to be placed onthe market have to comply with Regulation(EC) 503/2013 on applications for authorisation of GM food and feed.
To that end, applications for authorisation for the use of an Annex XIV substance for the production of such spare parts and for the repair of such articles should be simplified.
The transitional arrangements applicable to the substances concerned by those usesshould be extended in order to allow for the adoption of implementing measures for such simplified applications for authorisation.
Member States shall require applications for authorisation to be accompanied by a programme of operations setting out the types of business envisaged and the structural organisation of the credit institution.
To that effect,those wishing to apply for the authorisation or mutual recognition in parallel of biocidal products of that product-type containing no active substances other than existing active substances shall submit applications for authorisation or mutual recognition in parallel no later than the date of approval of the active substance(s).
(b) The Bank shall inform ESMA about the applications for authorisation that it has rejected, providing data about the AIFM having asked for authorisation and the reasons for the rejection.
Applications for authorisation, supplementary information from applicants and opinions from the Authority, excluding confidential information, shall be made accessible to the public in accordance with Articles 38, 39 and 41 of Regulation(EC) No 178/2002.
In the case of biocidal products containing more than one active substance, applications for authorisation shall be submitted no later than the date of approval of the last active substance for that product-type.
Applications for authorisation for these activities shall be submitted to the national authorities responsible for authorisation as referred to in points(a) and(b) of paragraph 1, and to the Authorisations Agency referred to in point(c) of paragraph 1.