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Medical Device Regulations and Quality Management System in Confluence
This live webinar will walk you through the basics of medical device regulations and how to build a compliant Quality Management System in Confluence with the help of SoftComply eQMS and the MediCompli Solution. We will show you how to implement ISO13485, IEC62304, FDA 21 CFR 820 compliant Quality Management System documentation in Confluence and how to add FDA 21 CFR 11 compliant document control workflows in Confluence.
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Webinar is over, you cannot register now. If you have any questions, please contact Webinar host: Marion Lepmets.