Examples of using Should submit in English and their translations into Slovenian
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Financial
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Computer
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Official/political
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Programming
Post-authorisation efficacy study(PAES): The MAH should submit the final study report for study P002:
The applicant should submit the final study report for Phase 3 extension study GS-US-312-0117,
Member States should submit information on permits issued for storage facilities as well as on the application
The MAH should submit the final study report to the CHMP and consider the need for a submission of a variation to the SPC for
The Commission should submit a report on the application of this Directive
The MAHs should submit all existing data that could demonstrate the efficacy of sodium salicylate when given to calves
private investment to N& N, and should submit regular reports to the EP and the Council on
Post-authorisation efficacy study(PAES): The MAH should submit an updated OS data for Study CA209017:
Post-authorisation efficacy study(PAES): The MAH should submit the final Study report for study CA209037:
Member States should submit reports on the implementation of this Directive on the basis of questionnaires drawn up by the Commission pursuant to Council Directive 91/692/EEC of 23 December 1991 standardising
Post-authorisation efficacy study(PAES): The MAH should submit the final Study report for study CA209067:
The MAH should submit the preliminary results of Study 20120325(a phase 2,
Those investment firms should submit an application for authorisation as a credit institution at the latest when the average of their monthly total assets is equal to or exceeds any of the thresholds set out in point(1)(b) of Article 4(1) of Regulation(EU) No 575/2013 over a period of 12 consecutive months.
the claimant should submit the court decision to have it recognised
Those investment firms should submit an application for authorisation as a credit institution at the latest when the average of their monthly total assets exceed any of the thresholds set out in Article 4(1)(1)(b) of Regulation(EU) No 575/2013 over a period of twelve consecutive months.
Post-authorisation efficacy study(PAES): The MAH should submit a molecular analysis in tumour material still available from patients treated in study CLDE225A2201 experiencing disease progression
In addition, the Commission should submit within three years after the entry into force of the new regulation a report examining the possible extension of the compulsory labelling of the country of origin to other products(milk,
You should submit your complaint.
Who should submit a request.
Author should submit two files.