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and the variability and heterogeneity shown by the protocols of the selected ELISA kits

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(All committee members underwent the same ethics review and vetting process required of all FDA advisory committee members, Emily Hilliard, a spokesperson for the Department of Health and Human Services, told me in an email.) The decision is only a recommendation, and the FDA would still need to sign off on an actual rule change

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What intermolecular interactions would be gained in the solution