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The FOIA can be used with the FCC but it will take a subpoena to get the information from CBS.
If the names show up to be the same people that complained to the SEC, things could get messy for a few people very fast after FDA approval.
Stay tuned.
Don't touch that dial.
We will be right back after this commercial.
Right after I sell?
I'll let you know.
One could only hope.
Everyone is entitled to their own opinion even if it's wrong.
Total or just for Covid-19?
Yes, not sure if that is east or west coast time but the office is in California.
No specific time referenced so............
Is it Sunday evening?
I saw it as a way to level the playing field between retail, shorts and flippers.
I think there are a lot of posters here that are like the blind man describing the south end of a north facing elephant.
We shall see soon enough what the whole elephant looks like from the distance of time.
Did any of those companies have an EUA number?
I believe the $6.95 number bantered around here is the cost to the CVS, rite aide, Dr offices ie professional package. The home test kit was $27.95 I think earlier from a press release.
But I'm probably wrong.
Hind sight is or should be 20/20.
I read this as the boat is scheduled to depart Thursday. Get your tickets and get on board for a coronavirus cruise that ends with everybody better than when they started when the boat returns.
All Aboard!
:}
The earth resonates at 2-3Hz with its 7th harmonic dominate.
Ever wonder why US subs have 7 blades?
All the people that sold after market on Thursday and early yesterday appear to have made an emotional knee jerk decision. They may have an opportunity to get back in farther down the road, we will see.
One needs either to believe Cytosorb works or it doesn't.
I think it does especially after 80,000 Tx with no untoward effects.
Still not convinced? Start reading the case of the week reports and keep reading till you figure it out.
Then go ask an ICU RN or anesthesiologist how much fun it is to titrate: Nipride drip, nitroglycerin drip, epical drip, dopamine drip, and dobutamine drip while managing the fluid volume on a pt. with an intra aortic balloon pump..
If at that point you are still not convinced to buy CTSO then maybe this isn't the stock for you.
Buy CTSO for your children and your grandchildren.
Old news.
Some trials are on a temporary hold during the Corona Virus epidemic.
Makes sense to me.
An emotional knee jerk response spurred on by myopic micro vision.
Someone saw an opportunity.
CTSO
TORONTO, April 15, 2020 (GLOBE NEWSWIRE) -- Auxly Cannabis Group Inc. (TSX.V - XLY) ("Auxly" or the “Company”), a leading consumer packaged goods company in the derivative cannabis market, is pleased to announce that its wholly-owned subsidiary Dosecann LD Inc. (“Dosecann”) has entered into an agreement with Medical Cannabis by Shoppers Drug Mart Inc. (“Shoppers”), a subsidiary of Shoppers Drug Mart Inc., to become a supplier of cannabis products through its online platform. The agreement will see Auxly’s suite of products and brands, including chewables, chocolates, vapes and oil in a bottle, all developed and manufactured at Dosecann, available to consumers across Canada. Dosecann has completed its initial shipment of cannabis products to Shoppers.
“Having our diverse cannabis product offering with Shoppers allows us to reach a wide group of patients across the country with our quality, science-backed products,” said Hugo Alves, CEO of Auxly. “We are proud to partner with Shoppers and look forward to bringing their customers our products, built on Dosecann’s pillars of quality, safety and efficacy.”
Greg Boone, CEO of Dosecann, added: “Our team at Dosecann prides itself on manufacturing products backed by science and advanced research and development to ensure that consumers get the high-quality cannabis products that they need. We think this achievement is a testament to the extraordinary team that we’ve assembled and the rigor and precision that we apply to product development and manufacturing.”
The agreement is for a three-year term, subject to renewal for an additional two years.
ON BEHALF OF THE BOARD
"Hugo Alves" CEO
Not quite true.
There have been four EUA since the 10th.
The rubberband has been wound up tight.
Time to let her go!
Tha 20,000 seems low. Thats only 222 filters a day on a 24x7 basis.
That's under 10 filters per hour.
What PR?
Do we have a number for production capability for 24x7 operations?
1 in 77 odds for which testing device are you referring? Version one for active or the improvement of version two for either IGG or IGM?
Tomorrow we will receive FDA EUA Approval.
Can you post a link?
Or are you setting this up for a tank when it doesn't arrive when "postulated"?
That would be correct. Finer point is that that is a SECOND method. It is my understanding and Could be wrong but its the FIRST test that received the approval from FDA. That test is not serology the second one is.
Help, someone that does know.
I am finding it easy to confuse the two as well.
They are both finger stick..........I thimk?
With all due respect My comment was more a comment as to whom you were addressing.
You may want to do some serious DD on Plutonium.
Hint.
Your preaching if not to the Pope at least to a cardinal.
Of course that is just an opinion.
Happy Easter
Do your DD.
Know your market.
Thanks for the info. So at what point in that cascade do you put in a double lumen catheter and start CytoSorb?
Cytosorb should be the standard of care in the ICU. If you have the virus, you are in the ICU, you are getting intubated because your lungs are filling up, You get a CytoSorb cartridge in that order boom boom boom. Get them in and out of the ICU quicker. Its that simple.
Sure we do:
dounome, orangecat, dr_lowenstein, Good Sport
In fact one is the new sheriff in town.
He can probably help.
Gosh if we only had a test that took 15 seconds. Ah well maybe someday in the future.
For those in search of the HOLY GRAIL (FDA approval) take note. We have found the paten it sat on.
They come as a set I would think.
paten: In many Western liturgical denominations, the paten is typically either a simple saucer-like plate or a low bowl. A smaller style paten will often have a depression that allows it to securely sit on top of the chalice. (Hemodefend)
Enjoy all your Easter celebrations.
One would hope it leads to fast trac approval.
To soon to correlate EUA with normal FDA approval.
Damn straight it works. 80,000+ times it works.
https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations#covid19ivd
Barring a curve ball from DECN I believe we are looking for approval for whether you are active with the virus. Phase two would either be the same test for at home use or the antibody test. So three potential game changers. One step at a time.
Extracorporeal Blood Purification Devices
There is now one listed on FDA EUA site.
Are we next?
https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/emergency-use-authorization#2019-ncov
If the FDA likes the tech. we should be next.