Real-world evidence (RWE) is everywhere in healthcare conversations — but what does it actually take to make it work in practice?

In this Medical Device Innovation Consortium (MDIC) Summit luncheon session, leaders from Premier Applied Sciences break down how high-quality RWE is generated, validated and used to support regulatory submissions, medical device innovation and evidence generation at scale.

This is not theory. It’s a practical look at how connected data streams, health system relationships and regulatory-grade methodologies come together to produce evidence that stands up to scrutiny — and drives real impact.

Hear directly from industry leaders:

In this session, you’ll gain insight into:

• What separates “buzzword RWE” from regulatory-grade evidence.
• How linked clinical, operational and supply chain data creates deeper insight.
• Why data quality, completeness and representativeness matter for submissions.
• How chart review and validation strengthen outcomes when structured data falls short.
• Real-world examples of how RWE is being used in Food and Drug Administration (FDA) and global submissions.
• How organizations are combining technology, expertise and health system partnerships to scale evidence generation. 

Why this matters now:

As regulatory expectations evolve, the bar for RWE continues to rise.

Success now depends on more than access to data. It requires the ability to connect data sources, validate findings and generate evidence that reflects real patients in real care settings.

This session explores how organizations are doing exactly that. 

Please share your contact information to view the on-demand webinar.