Medical device labeling in the EU continues to pose a challenge for manufacturers, who must create compliant Instructions for Use in all required languages. The term "e-labeling" refers to innovative means for providing Instructions for Use in an electronic format for medical devices.
Originally e-labeling focused on IVDs, since these are usually used by healthcare professionals in a clinical environment, however, the latest proposed revisions to Directive 93/42/EEC and Directive 90/385/EEC introduce amendments pivotal for e-labeling for other devices.
To find more information use the below mentioned weblink
Originally e-labeling focused on IVDs, since these are usually used by healthcare professionals in a clinical environment, however, the latest proposed revisions to Directive 93/42/EEC and Directive 90/385/EEC introduce amendments pivotal for e-labeling for other devices.
To find more information use the below mentioned weblink
http://blog.fxtrans.com/2012/03/ready-for-e-labeling.html
With medical translation, where peoples' health is at stake, you shouldn't be relying on something that could just leave you stranded at a critical moment.Translation should be done with the understanding that the exact meaning of a text in one language should be convey accurately in another. The result will be genuine content, not the mere shadow of an original one.
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