Joining Criterion Edge’s President Laurie Mitchell, is guest speaker, Queenita Fernandes, Medtronic’s Medical Safety Manager, Patient Monitoring & Respiratory Interventions. In this webinar, we discuss how to deploy systematic literature review in order to augment post market clinical surveillance, and share best tips on a robust systematic literature review process. Following this, our guest speaker shares an informative case study illustrating more.
How leveraging published data can help meet regulatory expectations and inform internal decision-making
Steps for conducting a methodologically-sound SLR
How data obtained through SLR can empower the successful execution of post-market surveillance activities, drive efficiencies and support regulatory compliance.
Who Should Watch:
Those Regulatory, Quality and Clinical leaders and regulatory writers who are tasked with the development, writing, review or approval of Clinical Evaluation Reports for EU MDR submission, or anyone interested in learning more about MDR requirements for CERs.
Who are the Panelists?
Laurie Mitchell, President | Criterion Edge
Queenita Fernandes, Medical Safety Manager | Medtronic
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