Group 336
MEDICAL DEVICE REGULATIONS & QUALITY MANAGEMENT SYSTEM IN CONFLUENCE
In this webinar we will provide you with a live demo of the SoftComply eQMS Solution on Confluence Cloud. This demo will focus on how to implement ISO13485, IEC62304, FDA 21 CFR 820 compliant Quality Management System on Confluence Cloud. We will describe how to finalize your QMS documentation with embedded guidance and how to manage FDA 21 CFR 11 compliant document approval, CAPA, Change Request and Training Management workflows with compliant e-signatures in Confluence.
FREE
1 hour
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Group 336
MANAGING RISKS IN JIRA AND REPORTING THEM IN CONFLUENCE
This live webinar will walk you through the basics of both project and product risk management in Jira. We will show you how you can manage project risks as well as product risks through Hazards Analysis as well as FMEA with the SoftComply Risk Manager app in Jira. We will also demo how to link risks with requirements and test cases, and how to report risks easily in Confluence. For previous recorded demo video, please visit our YouTube channel. This live webinar will walk you through the basics of both project and product risk management in Jira. We will show you how you can manage project risks.
FREE
1 hour
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Group 336
BASICS OF LINKING JIRA & CONFLUENCE TO ESTABLISH TRACEABILITY
This live webinar will walk you through the basics of building traceability between risks, requirements and test cases in Jira and Confluence. We will show you how you can manage medical device risks in Jira with the SoftComply Risk Manager app and how you can build custom traceability matrices in Confluence.
FREE
1 hour
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