Primjeri korištenja Reference date na Engleski i njihovi prijevodi na Hrvatskom
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Colloquial
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Ecclesiastic
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Computer
Reference date of the offence.
Eight hours from the reference date and time.
Each vial contains 6 mL of solution 6.6 MBq radium-223 dichloride at the reference date.
Body awarding the qualifications Reference date België/Belgique/Belgie.
Each mL of solution contains 1100 kBq radium-223 dichloride,corresponding to 0.58 ng radium-223 at the reference date.
Do I need to submit fee factors with reference date 31 December 2016?
P increases in the amount of loan financing receivables towards associated enterprises as compared to the amount of such receivables at the reference date.
Do we need to submit fee factors with reference date 31 December 2016? Yes.
The reference date of the balance sheet referred to in point(a) shall be the first day of the financial year starting on or after 1 July 2012, but before 1 July 2013.
Each vial contains 2-4 GBq at the reference date.
Then in 19 AD a specific reference dates a passage: he said that the Carni and Norici had been at peace since they were"stopped… from their riotous incursions…" by Drusus 33 years ago, which was 15 BC.
Each mL of solution contains flutemetamol(18F) 400 MBq at reference date and time.
All banks at highest level of consolidation supervised by the ECB at the reference date of 31 December of the preceding year are obliged to provide data regarding the fee factors to support the calculation of the annual supervisory fees.
Each mL of solution for injection contains 400 MBq of flutemetamol(18F) at reference date and time.
Emphasises the fact that the staff reduction agreed upon shall be based on the existing staff and tasks as on the reference date of 31 December 2012 and that any new tasks of existing agencies or the set-up of new agencies have to be accompanied by additional resources;
The activity per vial may range from 400 MBq to 4000 MBq orfrom 400 MBq to 6000 MBq at the reference date and time.
Samarium(153Sm) lexidronam pentasodium: 1.3 GBq/ml at reference date. Corresponding to 20 to 80 µg/ml of samarium.
One multidose vial of 10-mL capacity contains 1 to 10 mL of solution,corresponding to 400 to 4000 MBq at reference date and time.
The requirements for submission of periodic safety update reports for this medicinal product are set out in the list of Union reference dates(EURD list) provided for under Article 107c(7) of Directive 2001/83/EC and any subsequent updates published on the European medicines webportal.
For the purposes of point(b), balance sheet total figures for calculating the ratio shall be based on year-end audited figures for the year before the year preceding the reporting reference date.
Each ml of solution contains 1.3 GBq Samarium(153Sm)lexidronam pentasodium at the reference date corresponding to 20 to 80 µg/ml of samarium per vial.
For the purposes of point(b), balance sheet total figures for calculating the ratio shall be based on year-end audited figures for the year before the year preceding the reporting reference date.
This ensures that the system is made more effective by avoiding a long time lag between reference date of the data reported, and actual date of reporting.
By way of derogation from Article 3(1)(a), for the months from April 2016 to October 2016 inclusive,the reporting remittance date relating to the monthly reporting of the additional liquidity monitoring metrics shall be the thirtieth calendar day after the reporting reference date.';
However, the marketing authorisation holder shall submit periodic safety update reports for this medicinal product if the product is included in the list of Union reference dates(EURD list) provided for under Article 107c(7) of Directive 2001/83/EC and published on the European medicines web-portal.
However, to facilitate the initial implementation of this Regulation by institutions and competent authorities, during the first six months of its application, the reporting remittance date relating to the monthly reporting of the additional liquidity monitoring metrics should be the 30th, instead of the 15th,calendar day after the reporting reference date.
The volume of water that has been used for irrigation on the holding during the 12 months prior to the reference date of the survey, regardless of the source.
The marketing authorisation holder shall submit periodic safety update reports for this medicinal product if the product is included in the list of Union reference dates(EURD list) providednof r under Article 107c(7) of Directive 2001/83/EC and published on the European medicines web-portal.
The fee factors should be submitted by close of business on 1 July of the current year, orthe next business day if 1 July is not a business day, with a reference date of 31 December of the preceding year.
The requirements for submission of periodic safety update reports for this medicinal product are set out in the list of Union reference dates(EURD list) provided for under Article 107c(7) of.