[FREE WEBINAR] Post-Market Literature Surveillance: Systematic Literature Review and Case Study
Click here to watch the recording of this webinar. Joining Criterion Edge’s President Laurie Mitchell, is guest speaker, Queenita Fernandes, Medtronic’s Medical Safety Manager, Patient Monitoring & Respiratory Interventions. In […]
[FREE WEBINAR] Clinical Evaluation: Measurable Objectives and Acceptance Criteria to Verify Device Safety and Performance
Click here to watch the recording of this webinar. This webinar is presented from the point of view of seasoned MDR-compliant CER medical writers. Criterion Edge discusses strategies for the […]
[FEATURED] FDA Updated Its eMDR System. Here’s What You Need To Know When Submitting Adverse Events
Executive Summary The US agency has completed planned modifications to its electronic Medical Device Reporting system – and added an extra field for MDR exemption numbers.
