Explore the strategic considerations at each stage of the development and validation journey to ensure that assays are both robust and compliant with appropriate global regulatory frameworks for prospective clinical trial stratification.
TORONTO (PRWEB)
August 24, 2021
There are many challenges and considerations in translating a biomarker to a molecular diagnostic test (clinical trial assay). When defining the intended use of novel biomarker, decisions including specimen collection, molecular content and platform selection can have a significant impact on a biomarker program.
Almac Diagnostic Services has substantial experience of analytical validation across all stages of diagnostic test development from utilization in early proof of concept trials through to IVD Companion Diagnostic (CDx) tests, often consulting to help guide biopharma companies through the process.
Register for this webinar to hear a series of case studies that explore the strategic considerations at each stage of the development and validation journey to ensure that assays are both robust and compliant with appropriate global regulatory frameworks for prospective clinical trial stratification.
Join Cheryl McFarlane, Assay Development & Validation Manager, Almac Diagnostic Services, for the live webinar on Tuesday, September 14, 2021 at 8am PDT (11am EDT/NA) to learn more.
For more information, or to register for this event, visit Clinical Trial Assay Development & Validation — Strategies for Success.
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