Member Info for Sangijuelas1

I now don't care what the SP is.

Time to sit back and leave it to do its thing

www.politico.eu/article/europe-testing-question-coronavirus-crisis/amp/

https://www.rapidmicrobiology.com/news/3-facts-hidden-behind-the-shortage-of-covid-19-rapid-antigen-test-in-eu

https://ec.europa.eu/commission/presscorner/detail/en/ip_20_2483

No mate I bought back at 214 after selling at 229 and 237.Very happy

Would you care to be out of this over the weekend?

Xxx

MMs desperately trying to hold it down

Morning, this is just the start!

Benben Anna Gross at the FT has covered a lot of the testing stories. Are you in touch with her?

FDA is not a progressive regulator. They are very bureaucratic and they haven't even approved our miraculous British AZN vaccine that has delivered us freedom to return to normal life.

That's what they will say

https://www.theguardian.com/business/2021/jun/11/half-of-clothes-sold-by-online-fashion-brands-made-from-virgin-plastic

There's clearly a big seller. They will run out sooner or later

It's to do with whether or not the trades are executed by an automated (A)process typically institutional and where a trade has been put through manually

The FDA has still not approved AZN vaccine so it will be easy for them to play it down by referencing the vaccines success

Just skimming through the SEC Reg statement from last month.

It makes reference to a listing for Accustem on the main London market, and there will then be ADRs listed on Nasdaq, presumably for the US investors.

It's all very confusing

Recommendations for Test Users, Health Care Providers, and Testing Program Organizers

Stop using the Innova SARS-CoV-2 Antigen Rapid Qualitative Test.
Destroy the tests by placing them in the trash or
Return the tests to Innova using the FedEx return label that was included with the recall letter that Innova sent to customers.

Warning letter sent to Innova

https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/innova-medical-group-inc-614819-06102021

"The FDA has significant concerns that the performance of the test has not been adequately established, presenting a risk to health. In addition, labeling distributed with certain configurations of the test includes performance claims that did not accurately reflect the performance estimates observed during the clinical studies of the tests. Finally, the test has not been authorized, cleared, or approved by the FDA for commercial distribution or use in the United States, as required by law".

https://www.fda.gov/medical-devices/safety-communications/stop-using-innova-sars-cov-2-antigen-rapid-qualitative-test-fda-safety-communication

The fox killer is on the case

https://mobile.twitter.com/JolyonMaugham/status/1403083478669869058

Yeah I mean Michael the 10% is just to give an example.

There's also the same sort of potential with the Bavencio collaboration