In this free webinar, the featured speakers will discuss the major labeling changes within the new EU MDR regulatory framework for medical devices. They will talk about important EU MDR labeling questions that manufacturers should consider, the importance of labeling and safety content translation, as well as how language service providers (LSPs) can ensure translated content is accurate and effective.
(PRWeb March 19, 2021)
Read the full story at https://www.prweb.com/releases/how_to_successfully_navigate_new_european_medical_device_labelling_compliance_upcoming_webinar_hosted_by_xtalks/prweb17808021.htm
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