Examples of using Reference date in English and their translations into Hungarian
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Financial
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Programming
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Official/political
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Computer
Reference date of the offence.
Eight hours from the reference date and time.
The reference date was 31 December 2017.
Each vial contains 2-4 GBq at the reference date.
Reference dates and technical specifications.
Each vial contains 2-4 GBq at the reference date.
In this case, the reference date of 6 months is appointed in court;
Radioactivity concentration of the product(1100 kBq/mL) at reference date.
The reference date is stated on the vial and lead pot label.
Certificate accompanying the evidence of qualifications Professional title Reference date.
Member States shall provide the Commission(Eurostat) with the reference date according to Article 3 of Commission Regulation(EU) 2017/712.
With the current password you can always query the state of your accountvalid on the last day of the previous month(reference date).
If the act was performed more than five years before the reference date, it can be reversed only if it related to one of the debtor's family members.
The notification should be transmitted before or together with the statistical data,i.e. by the 15th working day after the reference date.
For the purposes of paragraph 3, the Community reference date for products containing the same active substance or combination thereof shall be one of the following.
However, the NAV variable shall be updated for all investment funds on an annual basis,with a lag of maximum two months following the reference date of end-December.
For any given reference date, information on any new IFs or changes to the identification codes of existing IFs shall be transmitted first to the ECB, prior to transmitting NAV information.
The Commission is empowered to adopt delegated acts inaccordance with Article 8a determining those specific reference dates.”.
PSURs have to be submitted for allmedicines which are included in the EURD(European Union reference dates) list according to the conditions defined in the list(data lock points, submission deadlines and PSUR frequencies).
B 2. Reportingfrequency and deadline NCBs shall transmit to the ECB updates of the variables specified in Part 1 of Annex VII to this Guideline, at least on a quarterly basis, with a timeliness of two months following the reference date.
All payments shall be made by the last working day of each month, starting on the reference date or,where the reference date is not a working day, the last working day before the reference date. .
Reporting frequency and deadline NCBs shall transmit to the ECB updates of the variablesspecified in Part 1 of Annex VIII to this Guideline, at least on a quarterly basis, within 14 working days following the reference date.
Reference date' means the day or the days on which citizens of the Union must satisfy, under the law of the Member State of residence, the requirements for voting or for standing as a candidate in that State;
Insurers should use thetechnical information, which is based on market data related to the end of the last month preceding the first reporting reference date to which the Implementing Regulation applies.
The methodological framework(51 pages) included the main features of the exercise(e.g. scope,time horizon and reference date), and the assumptions made for the exercise(e.g. static balance sheet, zero growth and constant business mix) as well as technical guidance and definitions(e.g. different components of capital, how to deal with hedging positions, what to reflect in the evolution of profits and losses).
Marketing authorisation holders shall be allowed to submit requests to the Committee for Medicinal Products for Human Use or the coordination group,as appropriate, to determine Community reference dates or to change the frequency of submission periodic safety update reports on one of the following grounds.
A single assessment of periodic safety update reports shall be performed for medicinal products authorised in more than one Member State and, in the cases of paragraphs 4 to 6 of Article 107c, for all medicinalproducts containing the same active substance or the same combination of active substances and for which a Union reference date and frequency of periodic safety update reports has been estab lished.
Marketing authorisation holders shall be allowed to submit requests to the Committee forMedicinal Products for Human Use or the coordination group, as appropriate, to determine Union reference dates or to change the frequency of submission periodic safety update reports on one of the following grounds:(a) for reasons relating to public health;
( 1) of the European Parliament and of the Council on quarterly statistics on Community job vacancies, one regarding seasonal adjustment procedures and quality reports( hereinafter the« proposed regulation 1')and another regarding the definition of a job vacancy, the reference dates for data collection, data transmission specifications and feasibility studies( hereinafter the« proposed regulation 2').