Member Info for PL75

But but but it say 6 working days, nay 5 working days.....

You mean they can just reply whenever they feel like it?!

Oh ok, fair enough. I’ll just be patient unlike all the nappy wearing moaning whingebags

The odds are incredibly high. Why would they immediately announce sales? You’ve got to ink deals. Immediately placing it for sale obviously doesn’t equate to immediately selling.

Exactly Mikey. He's a man of his word. He clearly said, in May, that he'd get the test out as soon as possible during the summer. So let's look forward to June 21st when the countdown will truly be on. My bet is mid summer, whenever the feck that is

Zoom has said it. Who says it hasn't already happened? Another RNS just saying, yeah, they've got it wouldn't be that insightful given the confirmation below

'The Group expects to receive confirmation of the registration of the AffiDX® in-vitro diagnostic device in the coming days, which will allow the Group to immediately place the test on the market.'

Perhaps the moaners should now concentrate their efforts on 'where are the orders'

Anyone remember the good old days?

‘Well you wont get any more from me. You offer nothing

This board has become counter-productive for me. A waste of my time

Cheerio’

Struggling to see how that’s got anything to do with the price of fish when it comes to LFD procurement.

It’s entirely insane what’s going on though. They’ve flung out cash left right and centre for dodgy PPE and billions for tests from Chin-ah and then don’t pay their bills to U.K. companies.

When I said the coming days could be anytime from the next day up to eternity, I’ll be honest, I wasn’t expecting it to be closer to the latter.

Something is clearly going on. If it had been submitted for just a rubber stamp we’d have got it. Everything points to a more detailed look in relation to being the DHSC’s test of choice. Not much to do other than wait..... and wait.... and wait....

https://www.europarl.europa.eu/news/en/press-room/20210517IPR04111/eu-digital-covid-certificate-provisional-deal-between-parliament-and-council

€100m won’t get you very far.

It’s not brilliant Templar, it’s irrelevant spam

https://www.ft.com/content/14aedd1f-3f8d-4743-8eda-f40b3db3149c

https://twitter.com/manxmarkets/status/1395450941218951175

Or google ‘vaccine passports set for use ft’ - I’ve no idea why they bother with a paywall.

Basically the test events have gone well so they fancy getting a passport in place for bigger events. It’ll include proof of a recent negative test

Our saviour first posted just before midnight, so it’s definitely today. Fingers crossed!

Tomorrow Mikey - 100% nailed on. Quote me on that

https://bidstats.uk/tenders/2021/W20/751108476

https://dna-diagnostic.com/products/human/covid-19/
https://dna-diagnostic.com/news/new-cco/covid-19-antigen-test-kit-on-official-english-list/
https://www.gov.uk/government/publications/assessment-and-procurement-of-coronavirus-covid-19-tests/outcome-of-the-evaluation-of-rapid-diagnostic-assays-for-specific-sars-cov-2-antigens-lateral-flow-devices

Nothing that we haven't seen before as they were on the previously announced govt list. Just confirmation that the UK govt have paid this Danish company £15k for their tests for validation prior to selecting a sovereign test. Oh, hang on...

In other news, as expected, it's not as good as the gold standard world beating AffiDx

That's all well and good gmcc, but they haven't announced a CE mark, they've announced the Declaration of Conformity for CE mark. We're still waiting. If we had the CE mark, we're back to the original question in this thread, why aren't we selling - immediately?

Was that an apology as you were wrong? Are you arguing with govt guidance that's clearly written in black and white? You'd better tell the gov they've got it wrong.

Who says we're selling in to the EU? I agree with CO, looks like we're selling in to the UK

Avadog?

No, thank you... as the guidance says:

- the EU no longer recognises UK Notified Bodies
- UK Notified Bodies are not able to issue CE certificates (other than for the purposes of the “CE UKNI” marking, which is valid in Northern Ireland) - and have become UK Approved Bodies

https://www.gov.uk/guidance/regulating-medical-devices-in-the-uk

It’s not logic, we’d just need to also register it with an EU recognised body.

It’s not correct though. The U.K. aren’t a notified body for the EU anymore

I agree with BBN that they won’t be standing still. After all, if the MHRA RNS had landed this week this BB would have been filled with ‘where are the orders’ rather than ‘where is the approval’. Can’t wait!

Otherwise, yup, everything points to the govt. It’s just a shame they’re not in a hurry...