- Key steps involved in helping medical affairs transition to a more rigorous regulatory environments.
- How to evaluate talent gaps, team leadership composition, and process challenges of your product portfolio.
- Critical systematic literature review technology and experience required to ensure CER and PER submissions are audit-ready and compliant.
Who Should Watch:
- Medical Device & Diagnostics Professionals (from small-medium sized to large enterprises)
Who are the Panelists?
Laurie Mitchell, President | Criterion Edge
Dr. Imelda Omana-Zapata, Senior Manager, Clinical Projects | BD
Criterion Edge has the expertise and resources to do literature reviews for many types of documents. Ready for a free consult?
