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You say: "I don't think it is because it's a point-of-care test"
regarding the possibility that the current test on the patient solutions portal could be this pinner c19 rapid test.
Through the portal clinics and doctors could order the rapid test kits from pinner to do the POC testing at their offices, no?
MAYBE IS ARRAYIT'S MIDDLE NAME.
TOTAL LACK OF TRANSPARENCY
Just a possible speculative guess in the Mark/ReneTodd smoke and mirrors game.
WILD GUESS: The rapid test that pinner usa announced "pinner c19" (IgG/IgM) from China could have been acquired in collaboration with Arrayit.
(Pinner and Arrayit are already partners in the IgG testing world.)
I don't think pinner USA could have done it alone. They don't have the scientific credentials.
The current test on the patient solutions portal could be this pinner c19 rapid test.
Arrayit is developing a serological test. (see Utah ad)
ALL PURE SPECULATION DUE TO ARRAYIT'S LACK OF TRANSPARENCY
I'm confused now about what Arrayit is doing. The only way to find out is for them to make a public announcement. Everything else is pure speculation.
where did you see that
The problem is that they are selling a swab test. Arrayit's is a blood test.
Why didn't Arrayit agreed to be identified on the FDA website?
It's good that the FDA studies the validity and accuracy of the tests before approval.
You don't want too many false positives or false negatives
Do you have a list of the 80 or so labs that applied for EAU but are are still waiting for approval, but they can sell their test pending approval.
Over 100 labs have applied for the emergency approval but FDA has only approved 22 so far.
On the patient portal they added the covid-19 test for doctors to order the
test kits, so it must be offered
https://patientdatasolutions.com/
I see. Thanks
Which lab processes the covid test for Pinner?
Q: When will other diagnostic tests for COVID-19 be authorized?
A: More than 100 companies have requested and received the FDA-developed Emergency Use Authorization (EUA) template for diagnostics for this outbreak. This template will help to expedite the development and authorization of other diagnostic products under EUAs. The templates for these diagnostic testing EUA submissions are now available on our website. If you need additional information, please refer to the FAQs on Diagnostic Testing for SARS-CoV-2.
https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/coronavirus-disease-2019-covid-19-frequently-asked-questions
On your link, it says
Testing coronavirus survivors’ blood could help reopen U.S.
Serology tests for antibodies could show how complete and lasting immunity will be
https://www.washingtonpost.com/health/2020/03/31/coronavirus-serology-blood-tests/
Wrong. If they had over 10M in assets as of 12/31/19 they have to file a 10-K for 2019 within 120 days i.e end of April.
https://www.law.cornell.edu/cfr/text/17/240.12h-3
One year ago there were over 700. And just about everyday after that they would tweet new ones being added 'Aug 9, 2019
Arrayit clinical sales team announces enrollment of a new top healthcare provider in our Patient Data Solutions allergy testing portal"
Good explanation SD.
WHEN YOU SAID IN OTHER POSTS
FOR DOCTORS AND CLINICS TO ORDER THE TEST FOR THEIR PATIENTS
Maybe you don't understand that the FDA is allowing accredited labs to sell their test pending approval of their emergency application.
Please, no need to imply that any one can order the covid test online. The Patient Data Solutions is for doctors and clinics to order the test kits and to receive the results of the test there.
We all know that the Patient Data Solutions portal is used by only doctors and clinics. That's where the results of the allergy test and now the covid test are reported to the doctors.
If you click to learn more about the Medicare approved lab doing the allergy and the covid19 tests it goes to the Arrayit page.
https://patientdatasolutions.com/
Has to be ordered by a health professional.
Agreed.
One thing missing from the Arrayit covid-19 test pdf instructions is the health worker using gloves to get the blood samples.
http://www.arrayit.com/SARS-CoV-2COVID-19TestInstructions.pdf
I wasn’t aware of that.
Those companies have probably issued PRs.
Arrayit hasn't because of the form 15 they filed back in August they can't.
IMO
But Arrayit can still sell their test since they submitted an emergency application about 2 weeks ago.
You say:
If you read the instructions, it's geared to health professionals because the say "patient's". And a patient is a "person receiving or registered to receive medical treatment."
1. Wash the patient’s hands with soap and
warm water. Rinse and dry completely.
2. Wipe the patient’s finger tip with the
alcohol swab.
etc
http://www.arrayit.com/SARS-CoV-2COVID-19TestInstructions.pdf
You're welcome.
What Arrayit told you about their test agrees with what the FDA has stated.
a.available to doctors and clinics only, not directly to the public.
b. test is in circulation now while awaiting FDA emergency approval.
Arrayit sells two types of blood cards: One is for whole blood. The other separates whole blood into red blood cells, white blood cells and serum components.
IMO the first one, whole blood, does not require FDA approval and is the one being used for the allergy test and for the covid test.
The second that separates the blood does require FDA approval, and it says so on the shop.arrayit website
http://shop.arrayit.com/microarray-blood-test.aspx
http://shop.arrayit.com/blood_card.aspx
Nice test if you enjoy having a big swab stick up your nostril to touch the back of your throat.
Not impossible for blood tests.
SN: What does an antibody test do?