Examples of using Database should in English and their translations into Slovenian
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Colloquial
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Official
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Medicine
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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
Every record in a database should have a primary key.
The database should be complete and up-to-date in order to render the BTI system effective EU-wide.
The local and remote database should be one and the same.
The database should be accessible to the public via the Internet.
In this case the wordpress database should exist on the same server.
The database should contain all relevant information as regards the clinical trial.
The EESC believes that such a database should be for information purposes only.
A Union database should be put in place to ensure transparency and traceability of renewable fuels.
Browse to the storage location where the damaged or missing database should be, and paste the backup file there.
This database should show a hyperlink to each relevant competent authority in each Member State.
DISCLAIMER: Although the RESPONSE project makes aneffort to review the accuracy of data,"Drugs monographs" database should only be used as a supporting(analytical) tool.
Searching similar images in trademarks database should be available to any party that wants to register its own trademark.
That database should improve detection of adverse events and should allow and facilitate the pharmacovigilance surveillance and work-sharing between the competent authorities and other authorities concerned such as environmental protection agencies and food safety authorities both at national and Union level.
Recalls that this database should include information on all steps of the legislative procedure to facilitate its traceability;
The database should equally contain infor- mation on the follow- up of these irregularities(such as financial corrections imposed).
The pharmacovigilance database should take into account mechanisms for exchanging data with the existing national pharmacovigilance databases. .
The database should also include a human interface with a team able to answer questions on the US and EU sides.
That database should include mechanisms for exchanging data with the existing national pharmacovigilance databases. .
The database should enhance overall transparency, streamline and facilitate the flow of information between authorities and prevent multiple reporting requirements.
That database should improve detection of suspected adverse events and should allow and facilitate the pharmacovigilance surveillance and work-sharing between the.
That database should improve detection of adverse events and should allow and facilitate the pharmacovigilance surveillance and work-sharing between the competent authorities.
This database should include all relevant information for compliant and non-compliant products in order to avoid unnecessary testing in another Member State and should be user-friendly and easily accessible;
That central database should contain all the information set out in Annex V to Directive 2008/106/EC on certificates of competency and endorsements attesting the recognition of certificates of proficiency issued in accordance with Regulations V/1-1 and V/1-2 of the STCW Convention.
These databases should also help to match information on works with information on phonograms or any other fixation in which the work has been incorporated.
For example, comparables found in pan-European databases should not be rejected automatically.
National and EU databases should progressively use the same standards and compatible technologies to ensure the selective exchange of law enforcement data while taking into account the appropriate inter-linkages with international databases. .
Wholesale measures ensuring the inclusion of end-user data(both fixed and mobile) in databases should comply with the safeguards for the protection of personal data, including Article 12 of Directive 2002/58/EC(Directive on privacy and electronic communications).
