Available for 90 days after enrollment
Approximate Course Run Time
Continuing Education Units
E-learning content is available on demand!
Over the next few weeks we will be adding five insightful webinars to this page, so please stay tuned as new webinars are published.
These five intuitive webinars will help you focus on various aspects of the MDR, from preparing a Clinical Evaluation Plan, to supporting you with preparing a Clinical Evaluation Report, with an in-depth, 2 - part webinar. Additionally, we’ll also give you advice around preparing a Post Market Clinical Follow Up Plan and Evaluation Report (PMCF) as well as helping you to understand how best to produce a compliant SSCP for both healthcare professionals and patients.
Key takeaways and learning objectives
Topics covered in the Clinical Evaluation Plan Session:
- Device Description
- Similar Device Data
- Clinical Claims
- Literature Searches
- Updates and Competency
Join Richard Holborow, Global Head of Clinical Compliance, as he talks about preparing for a clinical evaluation report.