A special order item will need to ship to our warehouse from the manufacturer before then shipping to you. The estimated delivery range that you see is based on the information that we receive from ...

Nuclein 在新闻稿中表示，DASH 快速 PCR 系统和 DASH SARS-CoV-2 和流感 A/B 测试将于本月晚些时候上市。 参考来源：‘Nuclein receives dual FDA 510(k) clearance and CLIA waiver for DASH® SARS-CoV-2 & flu A/B test for use on the DASH® Rapid ...

The Supreme Court on Wednesday backed a series of decisions by the US Food and Drug Administration to deny market access for flavored vaping products in a rare win for government regulators that ...

In Q2 FY2025, the Company has made significant progress with its clinical trials in the United States for the US FDA CLIA-waiver of its FDA approved Reveal ® G4 HIV-1/2 rapid test. During the ...

and history” of the FDCA and CLIA make clear that the “FDA lacks the authority” to regulate laboratory-developed test services. Upon the Final Rule’s release last year, the FDA’s plans ...

The US Food and Drug Administration announced Thursday that it will be phasing out a requirement that monoclonal antibodies and other drugs be tested on animals, saying in a news release that ...

Genzen said LDTs existed long before either the FDA or the CLIA law. LDTs are operated by "highly skilled professionals who are either board-certified physicians or PhD-level laboratory scientists ...

‘Never yield’: Fareed Zakaria explains Chinese mentality over trade war ...

In Q2 FY2025, the Company has made significant progress with its clinical trials in the United States for the US FDA CLIA-waiver of its FDA approved Reveal ® G4 HIV-1/2 rapid test. During the ...