In this free webinar, attendees will gain insights into key technical, regulatory and commercial considerations when defining a companion diagnostic (CDx) strategy. Learn about how the clinical trial design can affect diagnostic development, challenges associated with working within a diagnostic–pharma partnership and how to optimize the partnership and build synergy.
TORONTO, May 6, 2024 /PRNewswire-PRWeb/ -- The partnership between a diagnostic provider and a pharmaceutical/biotechnology company is crucial when developing a companion diagnostic (CDx). It is important to ensure that the strategic approach for the therapy and diagnostic is aligned to achieve the same clinical, regulatory and commercial goals, as well as aligned with the program risk profile.
When developing a CDx, it is critical to define a clear and aligned goal and vision from the outset. Then, to determine the CDx strategy, the important technical, regulatory and commercial considerations need to be examined too. In fact, the clinical trial design can affect diagnostic development; therefore, there are many challenges associated with a diagnostic–pharma partnership.
In this webinar, the expert speaker will share recommendations on how to optimize the diagnostic–pharma partnership and build synergy. They will also explore some of the realities of managing CDx development programs with pharma and biotech partners from a diagnostic providers' perspective.
Register for this webinar today to gain insights into the realities of managing CDx development programs with pharma and biotech partners from a diagnostic providers' perspective.
Join featured speaker Laura Nelson, PhD, Associate Director, Project Management, Almac Diagnostic Services, for the live webinar on Tuesday, May 21, 2024, at 11am EDT (4pm BST/UK).
For more information, or to register for this event, visit Managing Biomarker/Companion Diagnostic (CDx) Programs with Pharma: A Diagnostic Company's Perspective.
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