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. https://www.parexel.com/solutions/access/real-world-evidence

1. HOW CAN YOU SUCCESSFULLY
INTEGRATE EHR AND EDC DATA?

2. 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.

3. 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

4. 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?

5. GET ANSWERS TO YOUR QUESTIONS
ON-DEMAND WEBCAST
Putting The ‘REAL’ in Real-World Evidence
ONLINE
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 >