Clinical laboratory equipment manufacturers’ lack of guidance for high consequence pathogen response is a critical weakness

Author:

Le Aurora B.ORCID,Figi Claire E.ORCID,Herstein Jocelyn J.ORCID,Iwen Peter C.,Buehler Sean A.,Lowe John J.ORCID,Gibbs Shawn G.ORCID

Publisher

Cambridge University Press (CUP)

Reference10 articles.

1. 1. Centers for Disease Control and Prevention (CDC) Division of High-Consequence Pathogens and Pathology. Diseases and specialty areas [Internet], 2022. https://www.cdc.gov/ncezid/dhcpp/diseases-specialty-areas.html. Accessed December 22, 2023

2. 2. Centers for Disease Control and Prevention (CDC). Guidance for U.S. Hospitals and Clinical Laboratories on Performing Routine Diagnostic Testing for Patients with Suspected Ebola Disease [Internet], 2023. https://www.cdc.gov/vhf/ebola/laboratory-personnel/safe-specimen-management.html#anchor_1670347531971. Accessed December 22, 2023

3. 6. World Health Organization (WHO). Lassa fever - Nigeria [Internet], 2023. https://www.who.int/emergencies/disease-outbreak-news/item/2023-DON463. Accessed December 22, 2023

4. Clinical laboratory equipment manufacturer policies on highly hazardous communicable diseases;Herstein;Public Health Reports.,2019

5. 3. Budryk, Z. Device manufacturers restrict service amid Ebola fears [Internet], 2014. https://www.fiercehealthcare.com/healthcare/device-manufacturers-restrict-service-amid-ebola-fears. Accessed January 3, 2024

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