Member Info for Trickymatters

Thx Preefty. Gonna tweet about this today.

I don't claim to be intelligent Guy Incognito. I know what qualifications I have earned. I have to keep challenging your abuse. Filtering your boring posts now though.

Didn't cut through last year though did it? I think we are close now but for big sales we need approval.

Great chance for everyone to reduce their average. They only took £1k of my buy limit order yesterday with high volumes. I will go again today. My average is coming down baby! WHO approval in process- unless anything has happened since yesterday? Once that lands we are all over Europe and on everyone's radar big time. The WHO have actually made very few approvals. And they haven't got a huge amount of applications currently in transit. But they have got GDR. I am going to start tweeting about GDR later today. Once I have made my buy.
If Preefty is there, can you share the WHO link again please mate? Thanks.

The link ýou shared was a commercial update. Not the evaluation process you dumb arse. CE Mark won't cut it for Europe. One of the most regulated environments in the world. You are too thick for words. Like when you couldn't understand that we can't sell in the US without FDA approval.

Everyone knows what a CE Mark is Guy. Just ýou and Gloria think you can con people with a document published in French. When there's an English translation available on the link you shared! Lol.

Lth73, not enough of a scandal yet really. We could do with even more pressure from MPs?
Public not responding much to that yet. It's outrageous but from our point of view we just need to be in the mix going forward? Which we will be. I am still buying at this price. I had felt I'd reached a limit but may as well reduce my average now.
Ooh. Mary Ramsay is saying most of our tests are lateral flow tests now. Nadeem Zahawi: we'll transition from pandemic to endemic with long term testing, surge testing to quash outbreaks. Vaccine passports? NZ. A number of countries want vaccine certification. That's why we developed the app- double vaccines plus testing. Discussing the events trial. We need to get the travel industry back on it's feet. We are getting a testing industry so we are resilient. We could have new mutations yes. Future proofing in all these ways.
Signing off. Time for another walk in the sunshine. GLA.

Final steps on the road to recovery include getting people who haven't had jabs to get them. We're getting a bit safer every day.
Dr Mary Ramsay. Thx to NHS and PHE. Been analysing data on Delta variant. 90% protection from 2 doses. Promoting other vaccines now, MMR, meningitis, HPV and flu.
Looking at cv19 positive cases from tests. Surge testing may account for today's high cases. Breaking the link on hospitalisations and preventing severe illness and death.
Dr Nikki Kanani. Bigging up vaccines. Not quite getting all of the vaccine hesitant people. But much better than before. Very big emphasis on encouraging everyone to get the jab.
Questions. Are the non vaccinated holding back the freedom of other?
Most people in hospital are under 65. Those in most danger are over 65. And it includes those who are partially vaccinated and unvaccinated.
I will leave it there unless there's anything substantial on testing.
Looks like it's going to be about getting as many jabs in as possible before the July review.

Nadeem Zahawi is leading.
Infections up to over 16000. Those with only 1 jab are still vulnerable to hospitalisations. That's why we delayed the end of lockdown. Second doses need to be done for over 40s. Promoting this.

Anyone watching? I am.

That we didn't meet their mad predictions so they could pay even less having spent all day, every day ****ging off their own investment, lying and attacking other investors, to buy in lower! Damn those trolls ain't got no shame!

Dominating the news today. Won't happen before the vaccines are done. Then it's going to be test, test, test. Let's hope the WHO finish processing the GDR application ASAP. Faster to produce, faster to process GDR's PCR tests. What's not to like? Sp is cheap as chips. Guy Incognito was waiting for 38p to top up. Lol. No wonder his nose is out of joint.
My buy is executing now at 49.5p. Hope they take it all, not just a partial transaction.
GLA.

Very damning! It was very opaque- the evaluation process. As shareholders we have shared 3 different specifications for sensitivity thresholds so far. One of which was 'very good ' LOL! Which is what Innova achieved after the initial 84%.
Been a shambles. We should all write to our MPs. Still makes me laugh/cry. The EDSAB report. Two pages. With a paragraph response to 'What have we learnt?' That you can't use filter paper to separate antibodies from blood. Which came out, after 5pm in November and then disappeared from the PHE site. I will share a copy again if anyone wants to send it to their MP as an example of how it's been.

Sorry I posted twice on the same subject. I sent the first 5 minutes ago- didn't show at first.

Preefty, thanks for sharing the WHO applications approved and pending. Interesting that WHO approvals are far fewer than the FDAs. If we get WHO we are through EU approval and on the world's radar. I think we already will be due to the Beckman Coulter partnership but that will seal it. WHO approvals to date include all the big names - eg. Primer Design, Abbott, several big Chinese diagnostics. Those pending are in the same league. And little old GDR! If the WHO are being choosy that suggests the market should start thinning out bit. There's so many poor quality players slowing down the world's regulators wading through everything.
So the WHO have GDR with an R status. Meaning they have requested additional information. I'll email Walbrooke today and ask where they are with that.
GLA.

Thanks Preefty. The WHO have the GDR application marked 'R' which means they have asked for information from the manufacturer. A quick email to Walbrooke anyone? If we get WHO authorisation we're through to EU approval and we'll be on the world's radar. They haven't approved loads of tests and they aren't considering that many either. Very much the very big pharma so far- Abbott, Primer Design, a number of the big Chinese firms and yet there's GDR. Exciting. I am buying more GDR this week.

Date McNumbskull. See my explanation to Gloria. Use the translation button.

Gloria, you can translate to English. That's not what it says. And there's a list of approved tests. Is GDR on it?

The biggest hit on sentiment is a falling sp. The facts are in our favour. New variants causing some anxiety has delayed the end of lockdown. But July 19th looks like it's firming up as the end game. Not before time.
All the advice we are getting from PHE is that we will always have covid as an endemic disease and the narrative is firming up too. We have to learn to live with it. And that means testing will replace isolation for contacts of those who have it. Two lateral flow tests will be followed up by a PCR.
The only way we hold onto an aviation industry is through testing. The EU certification scheme will mean more of a move towards the best in class and a less crowded field. Macron wants a standard for testing across the EU. The FDA will coalesce around standards for faster productivity and faster, high quality processing. Like GDR tests.
As soon as the really big news is on the near horizon this kind of manipulation on Aim kicks in. Can't we all recall the 30% drop in the SNP price the Friday before the results came in? It closed at 35p. On the Monday it opened at 80p. It hit £1 inside 2 minutes. I remember because I was trying to buy. Why do the market makers do it? They have little incentive in making it easy for us. If you put your money in a fund you pay fees. Why bother if people like us show that we can do it ourselves.
Within weeks we could easily see a double or triple bagger here. Buy or hold.

What don't you understand about 'the ECDC and the WHO are organising external validation for PCR tests '? The paper as a whole references several types of test.
Classic troll with the circular arguments. I know I'm not thick mate. I have an MBA and I worked for 15 years in R&D. I have finished the conversation with you. Wasting my time. Hopefully genuine investors now realise that we haven't got EU approval which is ongoing. I expect we will get it. I have bothered to explain this because you and others were insisting we hadn't sold in the EU despite having approval. Not true. When we get approval in the EU we can sell there.
Certainly the FDA criterion is very favourable to GDR technology.