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NEW YORK – The US Food and Drug Administration has been updating its guidance for COVID-19 diagnostic tests in a piecemeal fashion as the outbreak expands. On Wednesday, the agency held a webinar to flesh out its evolving policies, providing key insights on regulatory paths for molecular and serological diagnostic testing in commercial and state labs, and for commercial test products and devices.

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May
06
Sponsored by
Isoplexis

This webinar will discuss the application of single-cell proteomics and immune-imaging in adoptive cell therapy (ACT) for cancer.