ISO 13485 – QUALITY MANAGEMENT SYSTEM FOR MEDICAL DEVICES

[vc_row][vc_column][woodmart_title align=”left” woodmart_css_id=”6071c426a000f” title=”How ISO 13485:2016 can help you comply with EU IVDR” woodmart_empty_space=”” title_width=”80″ after_title=”Compliance with the new EU IVD regulation (IVDR) becomes mandatory in 2022. IVD medical device manufacturers can prepare by becoming certified to ISO 13485:2016, a key quality management system (QMS) standard that applies specifically to medical devices. Accredited ISO 13485 …

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