Dr. El Mustapha Bahassi, Associate Director of Clinical Laboratories at Medpace, highlights the biomarker landscape in immuno-oncology clinical research.
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Experts from Medpace’s central laboratory evaluated the effect of hemolysis, icterus and lipemia on chemistry assays and assessed the association between the amount of interfering substances and ordinal values reported by the automated chemistry analyzer as H-, I- and L-indices. They presented their findings at the 70th AACC Annual Scientific Meeting & Clinical Lab Expo in Chicago.
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Medpace offers global flow cytometry capabilities, with flow cytometry departments located at our US, Belgium and Singapore central laboratories.
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With an already robust menu of validated assays, the increase in new biomarker assay validations speaks to the seamless service we provide to our Sponsors.
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As part of our mission to deliver superb customer service and site support, we have recently expanded our kit building capabilities in the US and are currently expanding in the rest of the world.
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In this post, we highlight some of the key investments we have made in each of our biorepositories around the world and what that means for our Sponsors.
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With the advancement of precision medicine, molecular and genetic testing is becoming a critical component for patient selection and individual assessment of the risks and benefits of treatment. Known for partnering with sponsors at a very high-level of scientific engagement, the expansion of our molecular suite (1,975 square feet) further enhances our ability to support sponsors with advanced testing to detect pathogenic events at the genome level.
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Data from central laboratories have been key for assessing safety, tolerability, and efficacy of new drugs in clinical trials. With the increasing complexity and global scale of many clinical trials, it is important to maintain harmonization. Learn how we harmonize our data across our regional laboratories.
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As a full service, global CRO with an integrated central lab, Medpace has the scientific, operational and regulatory expertise to manage your celiac disease clinical trial.
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