Support Overview

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Point-of-care training and support

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Videos & Documents


Easy-to-access educational resources to support you throughout the process.

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Answers to the most common questions about the BD Veritor™ Plus System testing experience.

Designed with You in Mind

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BD Veritor™ System

Learn about Professional Care testing with the BD Veritor™ System.

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BD Veritor™ System Overview Brochure

Learn more about the BD Veritor™ Plus System.

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For additional training, equipment servicing, and more, contact our Customer Success team.

BD Veritor™ Plus System Education & Training

Discover the tools that enable you to streamline the point-of-care experience for those you serve.


Please visit our FAQ for more information on our testing capabilities and our products.

* The BD Veritor™ System for Rapid Detection of SARS-CoV-2 is intended for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in direct anterior nasal swabs from individuals who are either suspected of COVID-19 by their health care provider within the first five days of the onset of symptoms, or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between tests.

This product has not been FDA cleared or approved; but has been authorized by FDA under an EUA for use by authorized laboratories.

RSV=respiratory syncytial virus; SARS-CoV-2=severe acute respiratory syndrome coronavirus 2.

This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens.

This product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated, or authorization is revoked sooner.

 Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C §263a, that meet the requirements to perform moderate, high or waived complexity tests.  This test is authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.