Member Info for EmeraldCarrots

And I thought I was mad! LOL! If we make it to FDA approval in the USA we will be the ones laughing all the way to the bank as the saying goes............................................ 3 months? Application after CE approval for CYP2C19-ID Kit hopefully this week, so maybe 3 months from then!.

All IMHO.

A quite likely scenario within 12 months??

One I think. Will appear later otr sometin in the next 10 days.

Actually air fares not affected as I understand it. However WIZZ has got to be the safest bet for not being affected in the future if things get more nasty with a trade war. Not a lot the USA could do to WIZZ, is there.

Up 1%

0.5% up.

don't fly usa

FTSE bouncing

Analysis video. Dual DNA analysis of both circulating tumour cells (CTC’s) and fragments of DNA found also in the blood (called CtDna analysis).

https://www.youtube.com/watch?v=qaRjlUQ0uAU

Https://www.youtube.com/watch?v=-bU7dwjGBKU

Procurement System (DPS), permitting direct procurement by regional NHS trusts". So trusts can use their own budgets if need be. I think more Trusts will not wait for the NICE recommendation to roll the machine out throughout the NHS. Doctors & nurses at neonatal hospitals won't want to take the chance of making a baby deaf for life. The machine is being tested in "real life" situations at the 9 hospitals already, soon to be 14. Why take the chance?

All IMHO.

So it is a tad important!!!!!!!!

https://keystonecompliance.com/countries-that-require-ce-mark/

I think as long as we get the CE mark sign off this month as expected....... next week?

From 1st May (in use at 9 hospitals already) the data should accumulate rapidly.

Backing will make selling elsewhere easier. Simple as that.

Machine's installation in Scotland will drive/support sales of this vital machine. Sales surely MUST snowball!

" Scottish Government announcement of £800k investment to support national phased implementation program of pharmacogenetic testing of MT-RNR1 in newborn babies in NHS Scotland using Genedrive's MT-RNR1 ID ".

Https://www.ii-sa.com/genedrive-r-mt-rnr1

FDA application for the Genedrive® CYP2C19-ID Kit. Maybe why the sp has not moved yesterday or today.

Least at the moment. I'd sooner they concentrate on everything else:-

1. Getting the additional 5 neonatal hospitals set up with the Genedrive® MT-RNR1 to bring the total up to 14 hospitals.

- accumulating the "real life" data is vital for NHS roll out throughout the whole UK and potentially aiding the FDA application. The FDA application for this machine is financially the most important thing Genedrive have ever done. Tens of millions of $ to be had.

2. Dealing with all the additional enquiries for the Genedrive® MT-RNR1 which frankly must be happening now word has finally spread that without this test a newborn might be rendered deaf due to antibiotic reaction.

3. Getting the CE mark confirmed for the CYP2C19-ID and sorting out the RNS for the market.

4. Dealing with the additional enquiries from NHS trusts now the Genedrive® CYP2C19-ID Kit has been implemented into the Hyperacute and Acute Stroke Units of Peterborough City Hospital Acute Stroke Centre for routine clinical use. Pretty obvious more will follow this, and very soon.

All IMHO.

Application days later? Takeover??

"It's crucial to confirm that the cancer cells express HER2 before starting Enhertu treatment."

- ***Angle can do this*** from a simple blood sample DAYS before treatment starts to confirm! BUT I think red tape says this needs to be confirmed in a drug trial?? About time Astrazeneca opened their cheque book and got this confirmed. It is incredibly frustrating waiting for this to happen!!! They are so slow.

All IMHO.