Examples of using Normal time limits in English and their translations into Slovak
{-}
-
Colloquial
-
Official
-
Medicine
-
Financial
-
Ecclesiastic
-
Official/political
-
Computer
-
Programming
On grounds of efficiency, the normal time limits for the regulatory procedure with scrutiny should be curtailed for the adaptation of its Annexes.
On the grounds of efficiency and because of the time limits imposed by the procedures for calculation andpublication laid down, the normal time limits for the regulatory procedure with scrutiny should be curtailed for the revision of certain thresholds.
On grounds of efficiency, the normal time limits for the regulatory procedure with scrutiny should be curtailed for the adaptation of its Annexes.
When, on imperative grounds of urgency such as the urgent need to reinforce restrictions to the marketing oruse of dangerous substances, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to use the urgent procedure provided for in Article 5a(6) of Decision 1999/468/EC.
On grounds of efficiency, the normal time limits for the regulatory procedure with scrutiny should be curtailed for the modification of the Annex setting out the common criteria for consideration of an operating ban for safety reasons at Community level.
On grounds of efficiency, the normal time limits for the regulatory procedure with scrutiny should be curtailed for the adoption of the list of certain third countries.
On the grounds of efficiency, the normal time limits for the regulatory procedure with scrutiny should be curtailed for the amendment of the lists of certain categories of ingredients.
When, on imperative grounds of urgency, the normal time limits for this procedure cannot be complied with, the Commission should be able to use the urgency procedure provided for in Article 5a(6) of the above Decision.
When on imperative grounds of urgency the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to use the urgency procedure provided for in Article 5a(6) of Decision 1999/468/EC.
On the grounds of efficiency, the normal time limits for the regulatory procedure with scrutiny should be curtailed for the adoption of decisions concerning the selection criteria for the donor of tissues and/or cells and the laboratory tests required for donors.
When, on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to use the urgent procedure provided for in Article 5a(6) of Decision 1999/468/EC for the adoption of these tolerances.
On grounds of efficiency, the normal time limits for the regulatory procedure with scrutiny should therefore be curtailed for the adoption of those measures establishing additional feed additive categories and functional groups and for amendments to Annexes II, III and IV.
When on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to use the urgent procedure provided for in Article 5a(6) of Decision 1999/468/EC for the adoption of amendments of a purely technical nature.
When, on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to use the urgent procedure provided for in Article 5a(6) of Decision 1999/468/EC for the adoption of prohibitions, restrictions or particular requirements for certain products.
When, on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to use the urgent procedure provided for in Article 5a(6) of Decision 1999/468/EC for the adoption of a measure aiming to forbid the use of a vitamin or a mineral previously authorised.
When, on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to use the urgent procedure provided for in Article 5a(6) of Decision 1999/468/EC for the adoption of specific measures regarding the modification, suspension or revocation of Community authorisations.
On grounds of efficiency, the normal time limits for the regulatory procedure with scrutiny should be curtailed for the adaptation of the technical requirements related to storage, transport, distribution, quality and safety of blood, as well as requirements applicable to autologous transfusions, set out in Annexes I to IV, to scientific and technical progress.
When, on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission must be able to use the urgent procedure provided for in Article 5a(6) of Decision 1999/468/EC for the amendment of the list of materials whose circulation or use for animal nutrition purposes is restricted or prohibited.
When, on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to apply the urgency procedure provided for in Article 5a(6) of Decision 1999/468/EC for the amendment of the list of materials whose circulation or use for animal nutrition purposes is restricted or prohibited.
When on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to use the urgent procedure provided for in Article 5a(6) of Decision 1999/468/EC for the adoption of decisions concerning the selection criteria for the donor of tissues and/or cells and the laboratory tests required for donors.
When, on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to apply the urgency procedure provided for in Article 5a(6) of Decision 1999/468/EC for the adoption of decisions to amend the inclusion of an active substance in Annex I or to remove it from that Annex on basis of Article 13.
On the grounds of efficiency, the normal time limits for the regulatory procedure with scrutiny should be curtailed for the adoption of decisions determining the communicable diseases, the criteria for the selection of these diseases and the epidemiological and microbiological surveillance methods, as well as for the amendments to the Annex to Decision 2119/98/EC containing the list of categories of communicable diseases.
When, on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to use the urgent procedure provided for in Article 5a(6) of Decision 1999/468/EC for the adoption of the criteria and the procedure for the designation of the Registry as well as for the adoption of public policy rules concerning the implementation and function of the. eu TLD and the public policy principles on registration.
Consequently and on the grounds of efficiency, the normal time limits for the regulatory procedure with scrutiny should be curtailed for the adoption of general provisions regarding the application of the indications contained in the list of intended uses and for the adoption of amendments, in line with developments in scientific and technical knowledge, to the list of intended uses and the general provisions regarding the application of the indications contained in the list of intended uses.
When, on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to use the urgent procedure provided for in Article 5a(6) of Decision 1999/468/EC for the adoption of amendments to the Directive 1999/2/EC or to the implementing Directives by means of prohibitions or restrictions as compared to the previous legal situation to the extent necessary to ensure the protection of public health.
When on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to use the urgent procedure provided for in Article 5a(6) of Decision 1999/468/EC for the adaptation of the technical requirements concerning information to be provided to or obtained from donors, as well as requirements related to the suitability of blood and plasma donors, set out in annexes I to IV, to scientific and technical progress.
For this type of attachment,the period is ten years in the case of movable property(the normal time limit, because no special provisions apply) and six months in the case of immovable property(Article 1567 Judicial Code).
Article 2(6) of the proposal for a Regulation adapting a number of legal acts to Article 290 TFEU refers to the possibility of derogation butmerely provides that in duly justified exceptional cases the normal time limit within which the Council and Parliament may oppose the delegated act may be reduced to one month15.
The Commission argued that the complaint had been assessed within the normal time limit and furthermore that the information included with the complaint did not allow its services to clearly identify its object.