[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 certification from Globus Group is the first step on your regulatory compliance journey and lays the foundation for meeting your regulatory obligations.”][/vc_column][/vc_row]