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Navegar por los elementos (3 total)
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Autor: U.S. Food and Drug Administration (FDA)
Tema: Laboratory
Tipo de elemento: Publicación
Fecha de actualización: 2019-10-10
Descripción: This document describes the FDA's approval of the marketing of a rapid diagnostic test (RDT) to detect Ebola virus antigens (proteins) in human blood from certain living individuals and samples from certain recently deceased individuals suspected to…Example only: NETEC provides this item for reference purposes but does not endorse its content. Newer versions may be in place at the providing institution.
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Autor: U.S. Food and Drug Administration (FDA)
Tema: Infection Control
Tipo de elemento: Hipervínculo
Fecha de actualización: 2018-05-15
Descripción: Guidance information about Masks and N95 Respirators -
Autor: U.S. Food and Drug Administration (FDA)
Tema: Research
Tipo de elemento: Guía
Fecha de actualización: 2018-08-13
Descripción: FDA CDER statisticians are designing trials with adaptive features to make clinical evaluation of new drug treatments more efficient and informative. (FDA)More information on the subject can be read here.