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Foreign Clinical Trials
http://www.vanityfair.com/politics/features/2011/01/deadly-medicine-201101
From the info here, I will assume not.
Would CBIS have to file 8K, before FDA would lay legitimacy, to any of its claims ?
Is 8k needed for FDA approval ?
I do not understand the business of trading. I do understand CBIS
CBIS, is in a battle againt a machine, set up by power and greed, spurred by ego. IMO, Separation, is the intent. This saddens me because, separation does not exist. IMO, we are the cause of this. Cbis has the cure. Be Patient.
MMJ Legal, In our nations capitol. That is the power of TRUTH.
http://www.washingtonpost.com/blogs/mike-debonis/post/four-medical-marijuana-dispensaries-approved/2012/06/12/gJQAXHyhXV_blog.html
Study shows no evidence medical marijuana increases teen drug use
http://www.sciencecodex.com/study_shows_no_evidence_medical_marijuana_increases_teen_drug_use-93455
Bill To Regulate Medical Pot Clears Massive Hurdle
http://americansforsafeaccess.org/bill-to-regulate-medical-pot-clears-massive-hurdle
Did Eric Holder Lie to Congress?
http://americansforsafeaccess.org/did-eric-holder-lie-to-congress
Marijuana initiative appears headed to ballot
http://americansforsafeaccess.org/marijuana-initiative-appears-headed-to-ballot
As of March 31, 2012, the Company is re-assessing the license agreement with Rockbrook and how to move forward in a cohesive arrangement with the other license agreements and acquisitions the Company is working on.
http://www.rockbrookinc.com/
CBIS has many projects working. I am evaluating my co., by the focus they have put on prioritizing their projects. The A&E issue,is of lower importance to me comparatively. Although, if it is of importance to you, it would be to you to provide DD.
Buy all you can while at this low prices, as soon as FDA gives the go ahead POOOM $$$$$$$ See you all in another life
Why Legalize Drugs?
http://www.leap.cc/about/why-legalize-drugs/
DNA,,,How natural is that.
Ingredients listed, each product.
As time has passed, you,ve seen CBIS grow. You know, the power they have in store.
Fast Track, Accelerated Approval and Priority
Review are approaches that are intended to make therapeutically
important drugs available at an earlier time.
FDA can approve in as little as 3 Months
They do not compromise the standards for the safety and
effectiveness of the drugs that become available through this
process.
These revitalized FDA drug review approaches have yielded tangible results in bringing safe and effective drugs to patients with serious diseases more quickly. For example, since 1996, 68 drugs for cancer therapies have received priority review and approval.
FDA reviewed Gleevec, a treatment for chronic myeloid leukemia, in four months. Shortened review times have also brought promising treatments to patients with HIV/AIDS more quickly. Kaletra for the treatment of HIV/AIDS was reviewed and approved in 3.5 months. Pegasys, a combination product for the treatment of Hepatitis C was approved for marketing in 4 months.
Do they haf FDA approval ?
CBIS has truth I can't deny.
Cannabis Sunscreen = Billion Dollar Idea!
Reality: The THC levels in Industrial Hemp are so low that no one could get high from smoking it. Moreover, hemp contains a relatively high percentage of another cannabinoid, CBD, that actually blocks the marijuana high. Hemp, it turns out, is not only not marijuana; it could be called "antimarijuana."
DD Pls.
Cannabis Sunscreen = Billion Dollar Idea!
One of the main purposes of cannabinoids is to block UV light for the plants!
So rather than Oxybenzone and other crap causing cancer, Cannabinoids will prevent sundamage, prevent cancer and kill cancer all at once!
After curing cancer, this idea is enormous. Only about 10% of sunscreens are currently safe.
UVB causes dna damage and UVA causes ageing of the skin.
Cannabinoids block UVB and have anti-aging properties...
Life was made to work like this, we should all be greatful there are brilliant people like Dr. Bob to work this out for us.
The SUN gives CBIS POWER.
CBIS wants you to Vote.
Fast Track, Accelerated Approval and Priority
Review are approaches that are intended to make therapeutically
important drugs available at an earlier time.
FDA can approve in as little as 3 Months
They do not compromise the standards for the safety and
effectiveness of the drugs that become available through this
process.
These revitalized FDA drug review approaches have yielded tangible results in bringing safe and effective drugs to patients with serious diseases more quickly. For example, since 1996, 68 drugs for cancer therapies have received priority review and approval.
FDA reviewed Gleevec, a treatment for chronic myeloid leukemia, in four months. Shortened review times have also brought promising treatments to patients with HIV/AIDS more quickly. Kaletra for the treatment of HIV/AIDS was reviewed and approved in 3.5 months. Pegasys, a combination product for the treatment of Hepatitis C was approved for marketing in 4 months.
The table below illustrates the improvement in FDA review times in the years between 1993 to 2003. The median time required to review a priority review drug was reduced from 13.9 months to 6.7 months.
Fast Track, Accelerated Approval, and Priority Review have evolved over time. FDA has been vigilant in assuring that reducing the time necessary for drug development has not compromised the safety and effectiveness of drugs for patients with serious diseases.