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Excellent long term investment. It s way undervalued.
You lucky bastard. What was your entrance point? Lol
Holly shit mattysimone, this going to a dollar sooner than I thought! I know there is resistance... But it will come !
INVESTOR INFORMATION
Corporate Profile
ATWEC Technologies, Inc. is shaping the future of the daycare safety transportation industry by developing its patent-pending leading edge safety products relating to child transportation warning devices. Located in Memphis, Tennessee, ATWEC is publicly traded on the Nasdaq Pink Sheet as (ATWT). The company enjoys the privilege of being Tennessee’s first African American company to publicly trade stocks. ATWEC’s has incorporated into its program three components to establish the revenues. These components are Safety, Security, and Health. ATWEC is proud to announce that its Kiddiesystem products are leading the way in
daycare safety and transportation needs.
ATWEC’s goal is supply the daycare and preschool industry with all the latest technologies relating to transportation safety, vehicle tracking, security/fire alarms and video surveillance systems. ATWEC through its subsidiaries is also establishing great gains
in the security and bottled water industries.
SHAREHOLDER INFORMATION:
Exchange NASDAQ Pink Sheet
Ticker Symbol: ATWT
Cusip #: 050055 10 2
Company Information www.atwec.com
Fiscal Year End: August, 2005
Transfer Agents: Continental Stock Transfer & Trust Co.
Shares Authorized: 100M
Shares Issued: 8,000,000
Shares Free Trading: 2,500,000
52 week high: $ .25
52 week low: $ .05
Recent price: $ .13
Corporate Counsel: Zankowski & Associates Atlanta, Ga. 404-842-1434
CPA Rotenberg & Co. LLP Rochester, NY
585-295-0507
52 week high: $ .25 in 2005 ? What happened here ?
Questrade : $4.95 Canadian
Thank you glorifiedmantle ! I will have to open a chilean wine after reading this and ask myself why don't I have 1.2 mll shares like coloneco has...
The results they showed for patient one were not
A lab result doc. That's why . Docs are proof and proof are docs .it's ridiculous IMO, that they would release something like that. As soon as I saw it I knew the price was going down.
As you said, no signature...
How can positive biopsy results have little impact on a biotech ? Impossible. It' s like saying it's raining but humidity is not up.
Thanks to all for sharing your view on this !
Everybody has access to the FDA website. I meant to ask what your insight was on that . Do you think they could be approved for the fast track dev process, or most of all ; do you think they are Really going to apply for it ? I know it is just a guess ism kind of thing. But we all analyze investor' s sentiment and know that can drive the market too ...
Thanks!
I can't believe I sold @ 0.57. Darn
My father passed away after fighting cancer. Couldn't keep anything on his stomach. Too bad he didn't have the vapor back then. Never mind treating kids, infants... We will make lots of $$$$$$$$$. I know pills won't cease to exist.
Go RFMK !!!
I didn't say that at all. I am sure Pfizer would not want a competitor with a faster action pill. If you are in pain , which one would you choose ? honestly, eh ?
You can apply online. How long do you think it would take for us to get this confirmation ? What's your thought on this ?
Pardon me, I meant I need to confirm FDA got the application . Biopsy ( positive) will be a given then. And so our high profits
That would be awesome!
To make money. Like mining companies that let a claim expire... Sad ... I need to see the biopsy results. Most people do
" It takes over one hour for Marinol to reach full systemic effect, compared to minutes for smoked or vaporized cannabis."
How big is the market again ? Lol.
E-cig users and Thc e-cig users are Completely different markets!!! We are also talking about people that need the medical support from the cannabis but can't or won't be perceived as "Pot Heads".
FDA authorizes drugs with "I wanna kill my self " possible side effects. It ' s just insane all the resistance around medical cannabis.not to say ridiculous. I hope they have the biopsy. This will make everyone $$$$$$$$$$$$$$$$$$
RFMK, good night gorgeous ...
Have you sold ALL your shares today ?
Thanks for reminding me why I quit med school.
Thanks for your input. Do you think it will go bankrupt then, or just hiring a marketing expert would do it ?
Medical MJ is such a common thing in Canada. Can't
Believe the rest of the world will take forever to catch up with what is a human right : to have access to medical treatment.
Sorry . Not a small percentage. A dizimal one ,would make us all happy
Exactly! it's simple math. 7 billion people in this world. In a short term or in a long term small ( ? !) percentage of them will end up using the THC E-Cig. A small percentage of 7 billion. :)
How many regular cigaret brands are out there, just in Cali ? I know there is a 40 pages list with all the different brands.
It's too far out of reality to expect one single company selling it . It's no different with the THC E-CiG.
They actually inserted the "what if" because they would be sued if they named it cannabis cures cancer .
Documentary : What if cannabis cured cancer . Www. Amazon.com
Unless they apply for the Fast Track Development process...
It will go to a dollar. The company has "THE" product.
Fast Track development approval process. Would be nice if they applied for that. It accelerates the fda process : 60 days. But they have to prove Superior results to a disease that already has a treatment
60 days and $$$$$$$$$$$$$$$$$$$$$$$$$
iF they have a biopsy with positive results they could be granted fast track development. IMO
http://en.wikipedia.org/wiki/FDA_Fast_Track_Development_Program
THANKs again and again ! Lol
In Canada you can get a card " medical cannabis user " . They request your medical history , of course . Even back pain ... But the link is about the requirements for the Investigational New Drug: important regulations: you need their written permission to investigate here, there, and everywhere. Send samples to test patients in other states etc... Even to make the logistic of the trials viable and legal.
Mattysimone, THANKS!
Such a clinical investigation is not permitted to proceed without the prior written authorization from FDA. FDA shall provide a written determination 30 days after FDA receives the IND or earlier.