HOW CAN YOU SUCCESSFULLY INTEGRATE EHR AND EDC DATA?

Real-world pragmatic research has expanded dramatically as a tool to inform and guide the explanatory, pre-approval randomized clinical trials and to further assess product

value and risk-benefit.

Combining site-based research with healthcare databases offers significant cost savings and provides an innovate method to

generate real world evidence globally.

SITE-BASED RESEARCH

MORE EFFICIENT EVIDENCE

GENERATION

HEALTHCARE DATA ASSETS

YOU ARE PROBABLY QUESTIONING……..

Why are hybrid studies

important?

What are hybrid

studies?

What benefit can secondary data assets bring to your study?

What are the challenges

around accessing EHR and claims

data?

What are the critical steps in integrating EHR and EDC data within a real-world study?

What are the challenges

around accessing EHR

and claims data?

How can you overcome the challenges of

accessing EHR and claims

data?

GET ANSWERS TO YOUR QUESTIONS

ON-DEMAND WEBCAST

Putting The ‘REAL’ in Real-World EvidenceONLINE

This webinar will look at how companies can successfully navigate the EHR and secondary-data landscape, and design and implement studies that reap the benefits of combining EDC and EHR data to answer key questions – transforming the theory of real-world hybrid studies into reality. 

WATCH NOW >