Roundtable Discussion; The Future of Mineral Sands. Watch the video here.
Porter... agreed, this entry level is a bargain just 0.055 to buy. That's 10 fold discount from the IPO. Crazy peeps haven't picked up on this yet. When this hits 1p plus in the new year when news gets released of it phase 1 trials there's going to be limited stock available. Good Cash Balance and current M/C is ridiculously low.
There you go !!! 5.85p to 19p
Where is everyone here ?
Bought in today 5.85 p ....Having dropped so much over the year and talks of a contract all over the news this is one to watch.
requesting any interested party to raise £40-£70M as part of a solution was always going to end in tears
I have asking HL for my share certificate, having they inform me I was too late as the dead line was passed.
I spoke directly to Computershare whom inform me they were still taking instructions up to 19th August. I inform HL on the 17th Aug that they could still request. I received acknowledgment that my shares would be sent to me on a certificate.
Then yesterday I received a message they were not issuing the certificate.
HL have been very poor to keep us upto date and I have raised a complaint into the matter.
Still not heard anything since my last call on Monday
And at 262p, these AT almost impossible to buy , more shorts triggered
first thing this morning markets shown a spread 305 to sell and 246 to buy so I think the shorts are being triggered
decided to grab a few at 274.3p
bought 308
R.I.P Good bye dear friend.
Ricky whom passed away
Well was expected with placing as I mention funding towards end sept or oct if no sales revenue.
Although very strange that many of my posts were removed on 11th Aug when I mention that forward selling was going on in mist of funding / Placing.
Typical Aim. The fact that they had discounted the shares by 40% says it all. If our tests were as good as GDR claimed then we should of had a placing at £1 plus per share.
This will be hard to climb back up without sufficient News, Running out of money is never a good sign especially we were told at the beginning of the year that GDR were moving forward. Seem Budd must of sat in the driving seat backwards !!!
Quote from DB last RNS
'Full clinical validation on patient specimens is required for regulatory registration and/or other emergency listings. The Company is optimistic that this can be completed successfully and is targeting CE marking at the end of September / early October, with prospective patient sample collection already underway. The Company is targeting initial product launch in Europe.
I don't think we will get any news now till end of Sept/Oct ... see quote from DB from last RNS below.
Also there are 100's of other companies awaiting FDA approval therefore it would be impossible to know when GDR get notified. See quote from FDA
My only concern here as time drifts along to end of Oct. funding is going to be an issue as there is no way distribution will happen prior to then.
ALDYOR
Quoted from FDA listings which GDR are shown.
The commercial manufacturers listed below have notified FDA that they have validated and intend to distribute diagnostic test kits as set forth in Section IV.C of the FDA's Policy for Coronavirus Disease-2019 Tests. Where the Authorization Status is "FDA Authorized," the FDA reviewed and issued an EUA for the test after notification was given. Where the Authorization Status is shown as "Not FDA Authorized," the FDA has not yet reviewed the manufacturer's validation and issued an EUA for the test, and the test is included in this list to provide transparency regarding the notification submitted to FDA. The "Setting for Use" designation of "H" refers to a laboratory certified under CLIA to perform high-complexity testing. Certain developers have completed the EUA process prior to offering a test for clinical use rather than notify FDA under this policy. Tests that have been issued an EUA can be found on the EUA page.
If an EUA request is not submitted within a reasonable period of time, or if significant problems are identified with a test and cannot be addressed in a timely manner, the FDA intends to remove the manufacturer and test from this list, would expect the manufacturer to suspend distribution and conduct a recall of the test, and may take additional actions as appropriate.
grimshady
all I posted was ' very disappointed we have not received any revenue updates' Cash burn monthly won't be sustained beyond later in the year, Without revenue or update then funding will be required.
Whats lies about that !!!
Appears another one of my posts been removed again from yesterday !!!
So much for a balance view. It now confirms LSE can control the boards in favour of their positions therefore what's the point of this messaging board ?