-- The SARS-CoV-2 Rapid Antigen Test Nasal uses a nasal swab to quickly and
conveniently collect specimens from people suspected of having an active
infection
-- Nasal sampling allows for collection of the sample from the front area of
the nose instead of the nasopharynx resulting on a less invasive testing
experience for patients
-- The test also provides patients with the option to self-collect their
nasal sample
Roche (SIX: RO, ROG; OTCQX: RHHBY) today
announced it has obtained the CE mark for its new SARS-CoV-2 Rapid
Antigen Test Nasal. The test will be available in countries accepting
the CE mark by mid-February 2021.
In comparison to the existing Roche SARS-CoV-2 Rapid Antigen Test, the
SARS-CoV-2 Rapid Antigen Test Nasal collects the sample from the front
area of the nose instead of the nasopharynx, resulting in a simplified
and faster testing procedure(1) . This testing method can help reduce
overall patient discomfort, particularly in sensitive individuals such
as children, elderly people and/or people with disabilities.
Besides being less invasive, the test also provides patients with the
option to self-collect their nasal sample under the supervision of a
healthcare professional. Through reduced physical contact, this method
of testing can help to decrease the risk of exposure to the virus for
healthcare professionals. Whether the test could also be used without
supervision of a healthcare professional will depend on local regulatory
requirements. https://www.marketscreener.com/quote/stock/ROCHE-HOLDING-AG-9364975/news/Press-Release-Roche-announces-the-upcoming-launch-of-the-SARS-CoV-2-Rapid-Antigen-Test-Nasal-allow-32328198/
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