The technological benefits of e-labeling are recognized by the European Union; however, having labeling available in electronic formats cannot be achieved without some serious considerations. Throughout the course of our day we may frequently create and distribute electronic copies of documents as if it were second nature. The process of creating electronic copies of labeling is not as simple as merely generating an Adobe PDF document
The draft regulation sent to the WTO for adoption has specific guidelines regarding what types of medical devices can use e-labeling, what types of documents can be available in an electronic format, and what types of steps must be taken to mitigate risk. A copy of this draft regulation is available for download along with the summary of these guidelines presented in a report that is available for free download.
Download your complementary article: “Requirements for e-Labeling” now and learn what is required and what you must consider when you choose to make you labeling available in electronic format.