Currently global value dossiers are rigid in construction; they are large, often difficult to navigate word documents or…
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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.
Post-approval research provides data from a real-world setting that can help prove the value of your product. With these studies becoming increasingly important to decision makers around the world, addressing the complexities of accessing and integrating these data is key.
Regulatory & Payer Submissions