EN Part 11 was created to permit the adoption of new information technologies by FDA-regulated life sciences organizations, while simultaneously providing a framework to ensure that the electronic GxP data is trustworthy and reliable.
EN Part 11 was created to permit the adoption of new information technologies by FDA-regulated life sciences organizations, while simultaneously providing a framework to ensure that the electronic GxP data is trustworthy and reliable.
ID Bab 11 dibuat untuk mengizinkan adopsi teknologi informasi baru oleh organisasi ilmu hayati yang diatur FDA, sambil terus memberikan kerangka kerja untuk memastikan bahwa data GxP elektronik tepercaya dan dapat diandalkan.
Basa inggris | Wong indonesia |
---|---|
created | dibuat |
permit | mengizinkan |
adoption | adopsi |
technologies | teknologi |
organizations | organisasi |
framework | kerangka |
electronic | elektronik |
new | baru |
information | informasi |
data | data |
providing | memberikan |
reliable | dapat diandalkan |
the | dan |
to | untuk |
ensure | memastikan |
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