Ensuring market access for a cutting-edge medical device, bio-pharmaceutical agent or diagnostic test is crucial for the long-term viability of life sciences organizations. Industry leaders aspiring to expand their market access reach need to understand the factors associated with securing coverage from payers and providers, especially for multinational companies or organizations looking to expand into global markets. As the industry proceeds to embrace the need for real-world evidence (RWE), there is a rising demand for life sciences organizations to gain a competitive advantage by leveraging RWE beyond clinical trials. However, understanding when to leverage RWE and how to integrate it into the product life cycle can expedite your market access success.
Join Baker Tilly for an informative webinar discussing the importance of evidence generation for successful market access. In addition to discussing key considerations when building your evidence-generation strategy, our specialists will talk about the need for evidence-generation beyond clinical trial data. We will cover the crucial role RWE plays in helping pharma and medical device organizations enter global markets. Our team will also discuss how you can amplify RWE to create positive return on investment (ROI) for your organization.
There are no prerequisites for this webinar, and advance preparation is not required. There is no cost to attend this webinar.
A certificate of completion will be emailed to you four to six weeks after the event.
CPE credit: One (1) hour total credit
Field of study: Specialized Knowledge (SK)
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