Member Info for Cwalsh

@Jay, hang in there if you can , we are almost there.

Argh... posted the wrong like again, getting old ...:-(

https://covid-19-diagnostics.jrc.ec.europa.eu/devices/detail/925

Sorry, just releasided posted the same link twice . This is the test kit with CE - look at the device number :-)

https://covid-19-diagnostics.jrc.ec.europa.eu/devices/detail/1

Yes Jay, Trust your research and stay strong , we will have a very exciting next few months.

It’s bit unusual we get mention in Chinese website , it’s published on 12th April

“ The US FDA has issued more emergency use permits (EUAs) for new and updated equipment and EU regulatory agencies. According to data from the research company Globaldata, there are more than 140 new coronavirus diagnostic testing systems currently under development. The early front-runner American biotech company Lucira Health has obtained emergency use permission for COVID-19 home test kits in November; British biotech company Genedrive also notified the FDA to prepare to sell SARS-CoV test kits in the United States Genedrive 96 portable PCR machine.“

Original Article:

https://www.eet-china.com/news/202104121610.html

Translated to English :
https://yuty6zack2gtqisva7ihhiotke-adwhj77lcyoafdy-www-eet-china-com.translate.goog/news/202104121610.html

That’s for the automated lab test , we have CE for manual test .

Has anyone seen this list before ? It’s new for me .

2nd link says - Automated Lab based not CE marked yet.

https://covid-19-diagnostics.jrc.ec.europa.eu/devices/detail/174

https://covid-19-diagnostics.jrc.ec.europa.eu/devices/detail/174

Cheers Tricky, Not sure why my NYTIMES post disappeared.
Here it is again for all.

https://www.nytimes.com/2021/04/14/health/coronavirus-testing-variants.html

I believe PATH have not had Genedrive listed before , now it is , can someone confirm ( below link i have got it from NYTIMES) article I have quoted in earlier post .

https://www.path.org/programs/diagnostics/covid-dashboard-implication-variants-covid-19-antigen-test-detection/

I got this .

At Beckman Coulter Life Sciences, we continuously work to create innovative solutions that’ll optimize your genomics workflow. During this challenging time, our innovative solutions can help you create a seamless, automated workflow capable of research extraction and test setup for SARS-CoV 2 or capable of enabling research of COVID-19.

From sample receipt and RNA extraction to thermocycling and analysis, our fully automated genomics solutions have helped establish test sites globally for a broad range of customer sizes and testing requirements.

We can be a one-stop-shop for your genomics workflow needs. Our integrated solutions enable seamless sample processing, and our instruments touch every point of the genomics workflow.

Want to find out how our Echo acoustic liquid handlers can save you up to 80% on reagent costs? Or how our Biomek i5 liquid handlers can automate the RNA extraction process? Explore our fully automated viral RNA extraction and detection workflow, a new solution for SARS-Cov-2 research testing.

https://www.sagentia.com/markets/medical/diagnostics/

@Guy, You and your crew sit here whole day and reply to every single investors poster while I go out for a walk with my dog , You have a stressful and miserable day.

By the way the fact remains same ‘You are an idiot’ keep entertaining..:-) .

Cheers Preefty.

@Guy, You have serious issues , split personality and you are obtuse or deliberately obtuse.

I clearly know that you are posting from different accounts .

All rats in full force today .

@Guy,

Check my posts again.

I have said that , The guy I know confirmed that the EUA status on BC website for the product C73254 changed on 3rd April , did you get that right ? Espanyol ?? What an idiot, you wasted my sunny morning, I am all yours now ..

@Guy, Am I obliged to report to you ?? :-), let me tell you again .. 3 products on BC website don’t have the EUA status before 3rd April , one product C73254’s EUA status been updated to obtained on 3rd April , Usually someone manually changes the status with an approval from product manager , it’s not randomly changed. I m not here to convince you or not anyone else , If someone believed me and taken his financial decision then he is the biggest idiot , I am here to share what I know with fellow GDR investors , similarly others.

@Jace, Stop acting like a innocent , Do you know the difference between FDA Approval and FDA EUA Authorisation? Go find that out first .

Hi Sally, He blows hot and cold air at the same time.

Dear DrShort ,

Welcome to the Gutter.

Yours Truly,
Maestro,Guy,Jace, forgot other rat name.

Lol Sally, He is oncall for the weekend while his colleagues jaceorge and co on holiday to neighbouring gutter.

Change the country to US on top right hand of the website .