We could not find any results for:
Make sure your spelling is correct or try broadening your search.
Share Name | Share Symbol | Market | Type | Share ISIN | Share Description |
---|---|---|---|---|---|
Abingdon Health Plc | LSE:ABDX | London | Ordinary Share | GB00BLF79J41 | ORD 0.025P |
Price Change | % Change | Share Price | Bid Price | Offer Price | High Price | Low Price | Open Price | Shares Traded | Last Trade | |
---|---|---|---|---|---|---|---|---|---|---|
0.10 | 0.98% | 10.35 | 9.70 | 11.00 | 10.35 | 10.25 | 10.25 | 135,942 | 09:05:06 |
Industry Sector | Turnover | Profit | EPS - Basic | PE Ratio | Market Cap |
---|---|---|---|---|---|
Chemicals & Chem Preps, Nec | 4.05M | -3.45M | -0.0284 | -3.64 | 12.48M |
Date | Subject | Author | Discuss |
---|---|---|---|
04/11/2021 22:23 | Anyways I'm not the holder but just to windup pw I predict abdx will bag with in two weeks ... mark my words | amd75 | |
04/11/2021 22:22 | I know him well he does this to earn the livings. | amd75 | |
04/11/2021 21:43 | That is a total lie , first you was saying that their tests didn't work now you saying their test didn't get approval , for your information abc antibody test have ce mark for professional use and government bought these tests for professional use and government used these tests for some sort of study , so please stop talking some thing which isn't true . | amd75 | |
04/11/2021 21:40 | You should see what PatWhite writes at SYME BB | alancopone | |
04/11/2021 17:57 | steadyeddyGuy - "Are Biosure providing antibody tests to any pharmacies" All UK sales stopped for all Covid test equipment unless government approved. If Biosure products are not on the two links I provided then they are no longer selling to pharmacies or pharmacies to consumers from 01/11/2021. | pwhite73 | |
04/11/2021 17:54 | seG - "Why is this new regulation causing issues with UK suppliers of tests ?" Because many of them don't actually do what they say on the tin. "A Covid-19 testing lab accused of producing thousands of incorrect results has not been accredited by the UK's regulatory body, despite the government saying it was. Wolverhampton's Immensa Health Clinic is being investigated over a potential error with 43,000 negative results. The UK Health Security Agency (UKHSA) had said it was "accredited with all appropriate standards". But independent national accreditation body UKAS said that was not accurate. Neither Immensa nor its sister company Dante Labs have been through a lengthy, three-stage process for private testing providers, UKAS told BBC News. Testing work at the site has been suspended since the error was revealed." | pwhite73 | |
04/11/2021 17:48 | Amd75 - A condition of the ABDX contract with the DHSC was that the AbC-19 Rapid Antibody Test gained approval from MHRA. It never gained approval so the DHSC refused to pay. | pwhite73 | |
04/11/2021 17:41 | Where does it say they didn't work . I don't think that is the case | amd75 | |
04/11/2021 17:00 | Just to let you all know that PWhite73 is a lying scumbag with multi user signing in to the account he will claim to be looking after your interests but he is only here for his self importance, he advised selling NCYT at 50p and lost all of his money in Iconic Labs, because he has lost all of his money he believes that this makes him an expert. Go figure. Be very careful of his advice and basically don’t believe a word he says he is the king of cut and paste. | pwhite73 emergency responder | |
04/11/2021 16:39 | seG - The Medical Devices Act 2021 came into law specifically to shut down a multitude of UK companies that jumped on the Covid diagnostic band wagon. Some have created numerous tests others have gone as far as to hire factory space to manufacture. From 01/11/2021 none will be able to sell diagnostic equipment in the UK without the explicit permission of the DHSC or UKHSA. "The government has identified a market failure, which threatens to impact on the work to date in driving down levels of the virus. There is evidence that a number of COVID-19 tests available on the UK market failed to replicate their stated performance either in technical lab-based validation and when used in the real world. Information about the true performance of COVID-19 test products is not easily accessible and is often confusing and not comparable. This has left consumers and the public at large without access to information that would allow them to make informed choices about the tests they purchase and where they could be used. ...After considering the responses to the original consultation, we decided to take steps to lay a statutory instrument under the Medicines and Medical Devices Act 2021 (MMDA) to create a regulatory requirement for the mandatory approval of antigen and molecular diagnostic tests for COVID-19. This legislation passed through Parliament and became a legal requirement on 28 July 2021." | pwhite73 | |
04/11/2021 16:14 | P white lying scum | bigjock36 |
It looks like you are not logged in. Click the button below to log in and keep track of your recent history.
Support: +44 (0) 203 8794 460 | support@advfn.com
By accessing the services available at ADVFN you are agreeing to be bound by ADVFN's Terms & Conditions