Key Takeaways
- How to address limited clinical and performance data
- Learn how to adjust the Clinical Evaluation Plan to align with the regulatory strategy
- Understand the concept of data sufficiency
Who Should Watch?
Those Regulatory, Quality, and Clinical leaders and teams who are tasked with the development, writing, review, or approval of clinical evaluation reports for MDR submissions.
Who are the Panelists?
Dr. Sarah Chavez, Director of IVD & Scientific Writing Services
Stacie Beecham, Principal Medical Writer
Criterion Edge has the expertise and resources to do literature reviews for many types of documents. Ready for a free consult?




