10times
29 Apr 2021Ended

Webinar: The Value of Real World Evidence and Secondary Data in MedTech

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Estimated Turnout

upto 100
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Based on previous editions

Editions

Apr 2021

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Not Available
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IQVIA experts will examine how and why RWE is imperative in the MedTech industry and should be leveraged early in planning stages. The session will .. Read more highlight ways in which RWE studies can provide meaningful support for research, marketing, clinical, regulatory decision making, and more. Requirements for medical devices are evolving, making evidence-based decisions more relevant than ever, especially when it comes to proving safety, effectiveness, improved patient outcomes, and regulatory requirements. The use of real world evidence (RWE) to support market access decisions, reimbursement strategies, and comparative effectiveness has become increasingly imperative and far-reaching in the last several years. Various data assets, such as medical and prescription claims and electronic medical records (EMR), provide a rich resource in support of clinical evidence development across the medical technology industry. In this webinar, IQVIA experts will focus on the medical technology (MedTech) environment, examining how and why RWE is imperative and should be leveraged early in planning stages. The speakers will explore ways in which RWE studies can provide meaningful support for research, marketing, clinical, regulatory decision making, and reimbursement requirements.

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