Results for archives translation from Danish to Latvian

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Danish

archives & records management section

Latvian

archives & records management section

Last Update: 2011-10-23
Usage Frequency: 1
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Danish

med forbehold af godkendelse fra national archives and records administration (jf. 44 u.s.c.

Latvian

saskaņā ar valsts arhīvu un datu administrācijas (national archives and records administration) apstiprinājumu (44 u.s.c.

Last Update: 2014-11-15
Usage Frequency: 1
Quality:

Danish

api- og pnr-oplysninger vil ved udløbet af lagringsperioderne som beskrevet i punkt 8 til 10 blive destrueret i overensstemmelse med national archives act [2].

Latvian

api un pnr informācija pēc glabšanas termiņa beigām, kā tas aprakstīts 8. un 10. punktā, tiks iznīcināta saskaņā ar likumu par valsts arhīvu [2].

Last Update: 2014-11-07
Usage Frequency: 1
Quality:

Danish

vil enhver oplysning, der videregives, i medfør af privacy act, access to information act og national archives act blive destrueret eller returneret efter brug i overensstemmelse med cbsa’s og canadas treasury boards informationsforvaltningspolitik.

Latvian

saskaņā ar likumu par privātās dzīves aizsardzību, likumu par informācijas pieejamību un likumu par valsts arhīvu, visa atklātībā nodotā informācija pēc izmantošanas tiks iznīcinata saskaņā ar cbsa un kanādas finanšu ministrijas informācijas izmantošanas politiku.

Last Update: 2014-11-07
Usage Frequency: 1
Quality:

Danish

for at kunne betragtes som fuldstændig bør den tekniske dokumentation i passende grad omfatte de elementer, der er opført i dokumentet fra global harmonization task force »summary technical documentation for demonstrating conformity to the essential principles of safety and performance of medical devices (sted)«, samt yderligere elementer, som kræves i henhold til eu-lovgivningen, eller, for så vidt angår medicinsk udstyr til in vitro-diagnostik, »summary technical documentation (sted) for demonstrating conformity to the essential principles of safety and performance of in vitro diagnostic medical devices«, samt yderligere elementer, som kræves i henhold til eu-lovgivningen, jf. for disse dokumenters vedkommende http://www.imdrf.org/ghtf/ghtf-archives-sg1.asp.

Latvian

lai tehniskā dokumentācija būtu uzskatāma par pilnīgu, tai pietiekami dziļi jāaptver vismaz elementi, kas norādīti sarakstā vispārējās saskaņošanas darba grupas dokumentā “summary technical documentation for demonstrating conformity to the essential principles of safety and performance of medical devices (sted)” vai, attiecībā uz in vitro medicīnas ierīcēm, “summary technical documentation (sted) for demonstrating conformity to the essential principles of safety and performance of in vitro diagnostic medical devices”, skatīt http://www.imdrf.org/ghtf/ghtf-archives-sg1.asp.

Last Update: 2014-11-08
Usage Frequency: 1
Quality:

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