Member Info for Korda

CE mark for mologic antigen test!!

https://twitter.com/mologic/status/1342043262778044416?s=21

Likely because currently antibody tests are “unknown”

Due to not knowing how long antibody’s last from
Previous infection and also from the vaccine.

It could give people a false sense of safety and possibly spread the virus faster, there’s plenty of study’s happening regarding immunity length likely when some real info comes out.. antibody tests will be a real game changer in the fight.

No problem, would be nice to see an antibody video under the same format too.

I think after people start having the 2nd vaccine jab that’s when antibody testing will come into its own.

Certainly promising for the first half of 2021.

Hi tricky,
I recently asked PR regarding tect transfer this was the answer I received so it’s still going ahed if it Dosen’t come tomorrow.

If anybody can answer would we require a further MHRA approval for LFT under visitect brand or would mologic’s cover it?

“ Re. 3 – Omega haven’t confirmed the timing of the process but Colin King did say that he hopes to have this completed and available in the early new year and it would be sold under the VISITECT brand”

Further more for those asking whos LFD was approved today by MHRA here it is in Video form... and looking at pics I’d deffo say innova? Unless anybody can correct

https://www.gov.uk/guidance/covid-19-self-test-help

Correct faz highly unlikely it will be avct or even ODX at the moment.. these are the current 5 LFT’s being worked with/assessed

https://www.gov.uk/government/publications/sars-cov-2-lateral-flow-antigen-tests-evaluation-of-vui-20201201/sars-cov-2-lateral-flow-antigen-tests-evaluation-of-vui-20201201

Agreed walbrook recently commented
“ Any sales of the UK-RTC to third party customers would require UK Government permission once their demand for supply had been met.”

And there’s no sites currently selling the RTC test still so my opinion is still filling gov orders.

“ Separately, Thermo Fisher said researchers at the University of Oxford, which is partnered with AstraZeneca on another COVID-19 vaccine, are using its newly CE marked antibody test to quantify immune responses in a clinical trial.”Can anybody explain why this isn’t the Uk-RTC test that’s being used?

Rigby by all means filter me. I only post news/facts. And try and help anybody I can with information.

yet another new strain of the virus detected!?

Han**** to announce further news on vaccine and also testing.. lots of gov updates on LFT tests so might be a good hearing.

Correct John and that’s the reason the gov are behind them for a asymptomatic testing such as Liverpool as it’s finding cases they wouldn’t know about..

Further find is this
“ Five LFDs were tested. Each device is either in use as part of mass testing or going through the final stages of validation at PHE. Each device successfully detected samples containing the new variant.”

So we know some of the tests but the gov website is stating 5 LFD’s final stages hopefully mologic is within that.

https://www.gov.uk/government/news/rapid-evaluation-confirms-lateral-flow-devices-effective-in-detecting-new-covid-19-variant#history

I understand what exceptional use is.

But this is the reason why MHRA are taking the time in decisions for home testing.

“ Innova SARS-CoV-2 Antigen Rapid Qualitative Test’ dropped from 79% when used by laboratory scientists compared to 73% when used by trained healthcare staff compared to 58% when used by self-trained members of the public”

“ Due to the uncertainty regarding the interpretation of antibody results, these tests are not currently recommended for widespread use.”

It’s not negative rubbish it’s stating the difference in a trained member delivering tests

“ More than 130 types of LFD have been assessed and 20,545 evaluations completed. These assessments are ongoing, but one LFD has been prioritised based on performance, the ‘Innova SARS-CoV-2 Antigen Rapid Qualitative Test’.

8,774 validation tests have been performed to date to assess the Innova device.”

“ Ongoing review in real time for the ‘Innova SARS-CoV-2 Antigen Rapid Qualitative Test’ shows that the test had a specificity of 99.68% (that is, a false-positive rate of 0.32%), an overall sensitivity of 76.8%, and a sensitivity of over 95% for those with high viral loads.”

“ Innova SARS-CoV-2 Antigen Rapid Qualitative Test’ dropped from 79% when used by laboratory scientists compared to 73% when used by trained healthcare staff compared to 58% when used by self-trained members of the public”

Further evidence of LFD’s in care homes.. likely the press briefing will touch on these specs later

https://www.gov.uk/government/publications/evidence-on-the-accuracy-of-lateral-flow-device-testing/evidence-summary-for-lateral-flow-devices-lfd-in-relation-to-care-homes

Only thing your doing is clogging the board.. which Inturn investors can’t see real news posted. No supprise many have you filtered

Zengah selling to my tune??

I’m posting facts not Ramps. I’m invested here (LTH)

Your the one spouting a load of BS...

Yes volume is looking good for a change currently 3.2mill traded.

But people don’t buy in cause they see zengah say this is going places they buy in on facts and research.

And basically innova was first to market and cleaned up regardless of spec.

The spec for the mologic test hasn’t been disclosed yet..

Most expected it to be used due to being trialed within the airport testing but currently no further mention of it.

But omega have gone through with tect transfer so must be worth it?

“ The MHRA has issued an authorisation to the Department of Health and Social Care to allow the use of the NHS Test and Trace COVID-19 Self-Test kit to detect infection in asymptomatic individuals.

This is an antigen lateral flow test (antigen LFT) which can give a result in 30 minutes.”

Mologics antigen test is approx 15mins.

Innova is 30 mins

Did tell you back to the 50’s after the P&D

And the mologic antigen test would turn into the
Visitect antigen test under ODX.

Strap in? You adding more of that watery fuel to your rocket? As not is happening.. make sure your landing pad is clear.

Where’s the mologic antigen’s CE mark? That’s mentioned within the MHRA approval?