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Wow, press conference states over 2,000 labs participating in COVID testing
Big pot, ARYC could very very well be one of them!
haha, it's hard to believe ARYC is "one of the most corrupt, lying company around." All you need to do is proper due diligence and know your investment. Mark and Rene are not that type people, I've met them.
Have you?
FAQs on Diagnostic Testing for SARS-CoV-2
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Clinical Laboratory FAQs
Q: I am offering my own test under the new policy outlined in the Policy for Diagnostics Testing for Coronavirus Disease-2019. Do I report all my results as presumptive?
A: Under the policy outlined in the Policy for Diagnostics Testing for Coronavirus Disease-2019, the first five positive and first five negative results should be reported as presumptive and confirmed by an EUA authorized test. If all ten of these results are confirmed by an EUA authorized test, confirmatory testing for subsequent results is not recommended in the guidance.
Q: I am a clinical laboratory certified to perform high-complexity testing under CLIA. I have developed a SARS-CoV-2 test and want to begin accepting patient samples. What should I do?
A: Please refer to the Policy for Diagnostics Testing for Coronavirus Disease-2019.
The FDA encourages such laboratories developing tests to consider the validation recommendations in the guidance as they seek to validate their tests. If you pursue an alternate approach, we recommend discussing plans with us early, through the pre-EUA program. Please contact us at CDRH-EUA-Templates@fda.hhs.gov.
As noted in the guidance, once your test is validated and you are ready to begin clinical testing, labs should notify the FDA at CDRH-EUA-Templates@fda.hhs.gov and provide the name of the lab, lab director, address, and contact person. In the guidance, we recommend that you confirm the first five positive and the first five negative samples with an EUA-authorized test and include in your test report a statement that the FDA review of the validation is pending.
As stated in the guidance, the FDA does not intend to object to the use of validated tests for specimen testing for a reasonable period of time after validation while the laboratory is preparing an EUA request. The FDA believes 15 business days is a reasonable period of time to prepare an EUA submission for a test that has already been validated.
We strongly encourage laboratories testing under this policy to contact their state public health department as early as possible in the process (perhaps even before receipt of any orders or samples) to help ensure they have capacity for the validation testing described in the guidance and have the information necessary to support case investigations. We also encourage laboratories to be sure they are familiar with state and local laws mandating reporting of diseases and conditions of public health significance.
Q: I am a clinical laboratory certified to perform high-complexity testing under CLIA. Do I need an EUA if I purchase a CDC-qualified lot of SARS-CoV-2 test kit reagents and follow the CDC's protocol?
A: No, you do not need your own EUA if you use reagents from a lot that has been qualified by the CDC and follow the CDC's EUA-authorized protocol. Testing using the CDC's EUA-authorized protocol and CDC-qualified lots of reagents is considered to be testing done under the CDC's EUA. Labs performing such testing under the CDC's EUA should be aware of any applicable conditions set forth in the EUA.
Currently, reagents qualified by the CDC are being sold through:
Integrated DNA Technologies (IDT): https://www.idtdna.com/pages/landing/coronavirus-research-reagentsExternal Link Disclaimer
Biosearch Technologies: https://www.biosearchtech.com/products/pcr-kits-and-reagents/pathogen-detection/2019-ncov-cdc-probe-and-primer-kit-for-sars-cov-2External Link Disclaimer
Q: I am a clinical laboratory certified to perform high-complexity testing under CLIA. Do I need an EUA if I purchase a CDC-qualified lot of SARS-CoV-2 test kit reagents and develop my own protocol?
A: Yes. Laboratories that wish to develop their own protocol should refer to the streamlined EUA policy outlined in the Policy for Diagnostics Testing for Coronavirus Disease-2019.
FDA encourages laboratories to discuss their plans with us early, through the pre-EUA program. Please contact us at CDRH-EUA-Templates@fda.hhs.gov.
Q: I am a clinical laboratory certified to perform high-complexity testing under CLIA and am interested in developing a SARS-CoV-2 test. What do I need to do if I make my own primers/probes or order the individual components?
A: Please refer to the Policy for Diagnostics Testing for Coronavirus Disease-2019.
The FDA encourages such laboratories developing tests, whether using purchased components or making their own primers/probes, to consider the validation recommendations in the guidance as they seek to validate their tests. If you pursue an alternate approach, we recommend discussing plans with us early, through the pre-EUA program. Please contact us at CDRH-EUA-Templates@fda.hhs.gov.
As noted in the guidance, once your test is validated and you are ready to begin clinical testing, labs should notify the FDA at CDRH-EUA-Templates@fda.hhs.gov and provide the name of the lab, lab director, address, and contact person. In the guidance, we recommend that you confirm the first five positive and the first five negative samples with an EUA-authorized test and include in your test report a statement that the FDA review of the validation is pending.
As stated in the guidance, the FDA does not intend to object to the use of validated tests for specimen testing for a reasonable period of time after validation while the laboratory is preparing an EUA request. The FDA believes 15 business days is a reasonable period of time to prepare an EUA submission for a test that has already been validated.
Like!
I'll be buying at least another 50k shares Monday. I'm getting close to 7-figs - yeah!
No, just not yet announced, not fake.
Try again, try harder, no one is falling for shake and fake anymore.
Next week could be very exciting for ARYC shareholders.
Hope you are one of them
sticks and stones
you sound edgy, any reason why?
i'm about to pop a top! cheers!
ha
that comment must break some kind of rule around here
right?
400,000 share could be quite a windfall
why would you be so so negative, all the time?
do you really own 400k shares?
PPP - let's go ARYC!
There must be some $$$ in it for a tech smart company CLIA Lab Certified MEDICARE MEDICAID CERTIFIED COMPANY
Next week could be awesome!
How many tests are we talking?
300+ million???
that's a lot of $$$$
Does LHC Group do in home blood testing?
Would be easy with fingerstick test
LabCorp guy just said they are working with other LABORATORIES
This is getting really GOOD!!!
Was that WALGREENS top guy standing with TRUMP?
HMMMM, didn't ARYC work together via PR reporting a while ago.
Let's wait until this next phase is rolled out before counting out ARYC
It would be great to see a PR on Monday
Big bid on the board 1M
This is fantastic news
Of course ARYC will be included
Leaders in microarray tech
This is the Roche Diagnostics recent emergency approved test:
We are very pleased that our Roche Diagnostics-developed test to help identify novel coronavirus (SARS-CoV-2) today received an Emergency Use Authorization approval from the FDA and obtained IVD CE-Mark. The cobas SARS-CoV-2 Test is for use on the cobas 6800 and 8800 systems.
Hospitals and laboratories can now run the cobas SARS-CoV-2 Test on Roche’s fully automated cobas 6800 and 8800 systems, which are widely available around the world. These are high volume testing systems that deliver the fastest time-to-results, with the 8800 system able to provide over 4,100 results in 24 hours. This means that more tests can be done faster, bringing certainty to patients, healthcare providers, and communities across the globe.
IF ARYC has a test and it can run hundreds of thousands compared to just the 4,100 tests stated above, wow, that would be huge.
relatively speaking, most of the rest are too, if it makes you feel any better
Absolutely a different test. NO HELP AT ALL. AS USUAL
AS USUAL, ALL INFO TAKEN OUT OF CONTEXT.
UGH! SO SAD AND DEPRESSING
Stick around to find out
Get ur popcorn ready
i read where they said it is much worse than the flu. this thing broke in Jan and the number of places people infected travelled to and encountered others was out of control for a while and still out of control in some areas. kinda worse than the flu really
good luck trying to get everyone in need of tesing to go in and get blood draws at one of their labs.
Once the serology testing is rolled out, ARYC tech will likely be included since it can easily sample, test and report so efficiently. Cheaply
This is a HUGE opportunity for ARYC.
They may try applying next month once they are financially current
It's very possible
The Centers for Disease Control and Prevention is developing tests that could provide public health officials crucial information about how broadly the coronavirus has spread in the United States, even among mild cases or people without symptoms, the agency’s director said Wednesday.
The serologic tests, which are different from the ones used to diagnose active infection, would allow researchers to test the blood of people who were not confirmed cases of Covid-19 in communities where the virus spread. They would be designed to look for signs that people have mounted an immune response after being exposed to the virus.
CDC Director Robert Redfield told Congress that the agency is working on two of these types of tests. [color=red]“CDC has developed two serological tests that we’re evaluating right now so we can get an idea through surveillance what’s the extent of this outbreak, how many people really are infected,” he told a House panel. “That is being moved out now to do these extensive surveillance programs.”[/red]
CDC developing serologic tests that could reveal full scope of U.S. coronavirus outbreak
NPR article, last paragraph could be serology testing:
Scientists in China and Singapore have been using a different kind of test — one that detects antibodies in the blood. The CDC's version of this test is still being developed. "We do have a test working with some of the samples from the first patients," says Dr. Nancy Messonnier, director of the Center for the National Center for Immunization at the CDC. In a conversation with NPR on Friday she said, "As soon as we are sure about it, we will use it more broadly."
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ARYC could definitely be involved and what Mark has expressed to shareholders. WOW
I've seen a few posters copy their email update here recently. Seems it's been proven. As much as the Dan Brown RRBB letter was.
Right, figures it was a deception by the other side who does not want ARYC to succeed, for whatever odd reason.
Thanks for clarifying the whole issue.
Not an issue to me. I have no idea why. Obviously, you don't either.
It will settle in courts, I guess. No big deal is the reality.
as I read thru it, the liability is ~ 100k to ARYC and third parties.
a mere drop in the bucket once we see financials.
Financials cures all ARYC issues. Just produce them.
These stupid posts will then go away.
It's a penny stock! Of course, MOST of us are willing to take that chance.
Go buy some Apple, Google, or another big blue chip if you want low risk.
We are here for the big payoff. I got plenty of other blue chips.
This is the potential bonanza stock. Has been for years, still waiting.
Long on ARYC here.
That's great news to hear! Mark has always been a stand up guy when I've met with him.
It's really good he seems to be opening up a bit. Fins could be around the corner.
It happens to me too! I'm a positive guy too, don't understand.
some people just like to be sad and depressed.
Someone once posted Sad and Depressed in their posts, all day long. Guess it is so for some.
Not Longs, we're excited for what is to come. Go ARYC!
Did someone tell you there is no auditor on board?
Mark told me it would be announced the day they file post form 15. No announcement of new auditor would occur.
Who did you talk to?
nah, it's because Trump doesn't understand the math.
nice try
It seems Iconic strategy is:
Buy at beginning of week
Bash the rest of the week
Bash all weekend
Buy again on Monday
Iconic, holla!
Good post, it seems the same from my viewpoint.
Well, I don't know factually, just like you don't know if they are having issues today.
What I can say is the rent is a small small fraction of the expected current billings monthly, from the last reported numbers of $2M per week, which was a long time ago and likely up to $1M per DAY!
Keep up the negativity, it will not work on such a fine company.
This is great, seeing Green.
Kind of reminds me of similar feelings watching this one, "I love the smell of napalm in the morning..."
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Yep, I was upset at that time.
What did I do? I went and saw MARK at his office in SUNNYVALE, CA near the APPLE campus. We visited. He was very cordial and the conversation calmed me down.
Been long since the day I invested nearly 4 years ago.
Go ARYC!
I love how you like to think you are reminding us of something new. This game is getting pretty fun, you having fun?