Examples of using Data requirements in English and their translations into Croatian
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Colloquial
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Ecclesiastic
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Computer
Whereas data gaps in the case of low-risk biological pesticides primarily occur because the data requirements are designed for chemical plant protection products, and are thus unsuitable for low-risk biological ones;
Calls on the Commission to extend customs data requirements and include the exporter
enhance the completion of the harmonisation process regarding the data requirements and methodologies, in particular in the field of guidance documents on ecotoxicology
including the data requirements, was designed for the assessment
volume of the reservoir, and the data requirements are different for each region.
decision-making criteria and data requirements;
preparing the ground for adapting to new data requirements.
review data requirements in marketing authorisation procedures, simplify post authorisation requirements and review incentives for breakthrough medicines.
the providers of scientific advice in order to remedy the situation whereby data requirements were established essentially as a compilation of needs for individual stocks,
The status listed in the data requirement table below have no bearing on the fact that certain data is provided only where circumstances warrant it.
The data requirement tables in Title I to Title XXI include all the data elements necessary for the applications and decisions dealt with in this Annex.
Data requirements for stocks which are managed under EU legislation.
In addition, the adaptation of data requirements should be used to prevent unnecessary costs related to testing.
Data requirements for stocks which are currently not managed under EU legislation
timely access to data requirements.
The exact data requirements, including variables
in line with personal data requirements.
Whereas in particular there are major concerns associated with the incomplete harmonisation of data requirements and methodologies used that may hinder the evaluation process;
The application procedure for simplified authorisation of a biocidal product is similar to the procedure for national product authorisation except for the different data requirements.
The justification for the proposed adaptations to the data requirements shall be clearly stated in the application with reference to the specific rules in Annex IV.
