Member Info for Inphobe

Additional, sales were made to Beckman Coulter for initial commercial rollout. Making the entirety of your "failed to obtain any approvals or sell a single test in a pandemic" comment false and probably reportable.

https://www.lse.co.uk/rns/GDR/first-us-shipments-of-genedrive174-96-sars-cov-2-kit-3cef2co55fyf8fr.html

Posting manifestly misleading information on here is skating on exceptionally thin ice. Genedrive's PCR has received CE-ivd mark, and is to my knowledge authorised in Thailand, Malaysia, and South Africa

https://www.londonstockexchange.com/news-article/GDR/genedrive-96-sars-cov-2-kit-receives-ce-ivd-mark/14549970

General observation, but this IS a thing: https://www.investopedia.com/terms/p/poopandscoop.asp

Odd post. What makes you think people topped up right this moment? Not that there'd be anything wrong with that. I know I topped in the 60s and low 70s. Why are you trolling?

Likewise Jay. Been nice to bring the average down.

Yep, nice day overall, tidy bit of buying into close

Might I suppose be worth a view for insight into process

https://www.fda.gov/medical-devices/workshops-conferences-medical-devices/virtual-town-hall-series-coronavirus-covid-19-test-development-and-validation-04072021-04072021

(I'm encouraged to have seen approvals popping through pretty much every day on their mailing list since I signed to it last week)

Nudge into blue

Me too, just took a wee sensible bit more

Big one at 11.13am

Looks like Mr_panic and doooom1 are busy again this morning. Quel surprise.

Nothing has changed. Remain patient. Hope you all had a great weekend

Here's a PCR for you: Clinomics USA Inc., TrioDx RT-PCR COVID-19 Test not authorised on that list, authorised 4 Feb.

However which part of my posts did you not understand maestro? it was not a point scoring exercise, simply 'that list is outdated, here is another resource to keep you abreast'.

No idea why I'm responding, but OK. DiaSorin Inc. LIAISON SARS-CoV-2 Ag still shows not-authorised on that page. It was authorised 26 March.

As I say, that page is outdated (who knows, they may update it in the next five minutes, don't quote me), and I was pointing out that it may be useful to interested investors to sign to the FDA updates to keep abreast. Not to engage in some convoluted and pointless debate maestro.

For those interested, it can be done here: https://www.fda.gov/about-fda/center-devices-and-radiological-health/subscribe-cdrh-mailing-lists

That list is out of date. Best way to stay up to date on FDA notifications is to sign to their mailing list. Approvals now coming through regularly as far as I can see. Don't expect GDR to take long now, but we won't know 'till it's done.

Yes, positive LFTs will be followed by a confirmatory PCR as per uk gov update here. Whose PCR is another matter.

https://publichealthmatters.blog.gov.uk/2021/03/30/covid-19-reintroducing-confirmatory-pcr-testing/

Interestingly maestro, you were not mentioned by name there. But now that you bring it up....

https://www.griproom.com/fun/how-to-spot-fake-comments-on-stock-boards

FDA updating over last day about variants. They note to labs to:

'Be aware that molecular tests that use multiple genetic targets to determine a final result are less likely to be impacted by increased prevalence of genetic variants."

Bodes well for GDR approval imo. Seems they are alert to the current urgency with variant emergence. Time will tell of course.

https://www.fda.gov/medical-devices/coronavirus-covid-19-and-medical-devices/sars-cov-2-viral-mutations-impact-covid-19-tests

Thanks

Expect the GDR surveillance list will update when this variant has been through testing

Got a source for that?