EN 21 CFR Part 11
LV 21 CFR, 11. daļa
RU правило 21 CFR Part 11
DE 21 CFR Part 11
FR norme 21 CFR Part 11
Definīcija: A Food and Drug Administration (FDA) regulation, Title 21 of the Congressional Federal Record, Part 11. This regulation specifies the conditions and criteria for determining the validity and trustworthiness of electronic signatures and processes.
Microsoft Terminology 2023. Entry from the Microsoft Language Portal.
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