Member Info for Latino

There are in the right market at the right time with anti-microbial products, now armed with the illusive FDA approval, the company is now on cusp of major commercial deals...these deals should now come thick and fast as many manufacturers will now be desperate to get their hands on this product.

Cannot believe SP had fallen so low, considering on FDA RNS this opened around 12-13p and we fell to this level...absolute steal of a price, only possible in this market hence second chance!

33%

Should rise into close...as lot of news imminent. OR we may see RNS before or after close...FDA news can easily come after market close..

The only people with sour grapes today after that superb RNS are shorters/derampers..they know it’s over!

Could not have expected more, FDA announcement is imminent now all the media talk yesterday, so double whammy RNS possible today with FDA Approval coming later today...could be a transformational day today for NCYT..

Simply superb RNS...

Sorry - wrong board!

Just superb!

This is insane and worrying....! Especially when there is NCYT test kit ready to use now. What are NHS playing at?

Spot on...I was trying to help the poster with some searching questions to trigger intuition...! That’s why I say education or is it ignorance of the issue!

These were ‘swabs’ by the way from mouth and nasal...is this what was said by Ncyt on BBC last Sat?

You need to be educated fella....for a starter vaccine realistically 12-18 months away (source: WHO).

How do we contain in the meantime?
How do we know someone has COVID19?
How do we decide who to put in quarantine showing symptoms?

OR do you want to put everyone showing symptoms in quarantine for 14-28 days!

BBC - 7690 people tested for COVID19 in UK today..nasal and throat test and sent away..

How serious does it have to get? For authorities to give medics around the world the basic and the gold standard diagnostic test kit (100% reliable / CE Mark/ Gold Standard / 90min Results). This is the best product in the market and is available....give it them a fighting chance!

Coronavirus: Outbreak at 'decisive point' as WHO urges action

Coronavirus outbreak: House Foreign Affairs, CDC speak on COVID-19 response | LIVE

Just mentioned: Vaccine 12-18months re-iterated if all goes to plan, Phase 1, then Phase 2 Trials starting in summer. They have a conditate drug..

Only three US states can test for coronavirus, says public lab group

https://www.cnbc.com/amp/2020/02/21/only-three-us-states-can-test-for-coronavirus-says-public-lab-group.html?__twitter_impression=true

Twitter: Dr. Dena Grayson
@DrDenaGrayson
This patient with #coronavirus is from the #California SAME COUNTY where infected #DiamondPrincess passengers were evacuated, despite being critically ill with viral pneumonia.

CDC needs to DRASTICALLY expand its #COVID19 testing capacity now.

https://www.nytimes.com/2020/02/27/health/coronavirus-testing-california.html#click=https://t.co/dO5IfubRti

‘Nelllie investor’ lol Been in this game for just a few decades so I think I have some idea!

Also to say when ‘they have news they’ll RNS’, it would be outrageous and deeply concerning if they have no news to share don’t you think (significant additional orders / quotations) by now..

Like most investors, I think it’s now the right time to update the market, it’s been a few weeks and there has been a lot of speculation so now is the time to update.

With the CVID19 getting out of control and being on the verge of pandemic, and there being constant speculation about Significant orders (Telegraph)/JV/Roche/C-FDA/US-FDA/NHS approvals, it’s getting to the point where this zero silence is now getting untenable...surely company can’t wait another week pass without an update of some sort at least.

Get that they were maybe waiting for FDA so they can announce this with sales update in one RNS. But it’s now come to a point where I feel they need to update us...hope CEO updates us tomorrow.

Well done very good find..like this bit:

The CE Mark in the European Union and the FDA-approval process in the United States both perform the same functions, namely assessing the safety and efficacy of new devices. FDA approval, however, is significantly more expensive to obtain for a number of reasons:

1. The documentation required from investigators is much less efficient for FDA submissions than it is for the CE Mark.
2. The review cycle is about three times longer with the FDA.
3. There are almost always more rounds of questions with FDA-approval submissions than with those for CE Mark.