Key Takeaways:
- 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
Criterion Edge has the expertise and resources to do literature reviews for many types of documents. Ready for a free consult?
