Rising Biosciences Inc (RBII)

[StockRocket]

RSII business model confirmed today on CC...There model is sort of like OWCP's but without all the FDA guidelines, indications, submission, trials, and all the COSTS that going into getting a product ready to submit to the FDA...That is very risky, costly and may never earn a dime in profit or revenue.....NOW RSII will have A team of pharmacists, chemists, physicians, etc..will be creating pharm grade medicinal cannabis product with the highest quality of ingredients and calibrated with precise accuracy. All forms of cannabis, but mainly topicals, creams, and orals. ..No one in the industry is doing this with precise accuracy...they will be the first...They come short of announcing they will supply to NWAV clinics (Alternative Medicine Centers of America) but if you read between the lines, its pretty much a done deal....Robert Weber is the CEO of both and he basicly said they had to separate the disposing/compounding side from the patient/clinic side as per their lawyers due to regulations.

The buy the ingredients and compound them to the form, exact dosage, % of THC, and dispense.. There is NO FDA here...no patents etc...Millions of dollars and years for studies are NOT needed like OWCP...and they might not even get FDA approval for psoriasis ...10% get approved of submissions to the fda. Also...they have a built in customer base already in NWAV clinics....Alternative Medicine Centers of America. Robert Weber is the CEO of NWAV and RSII. http://www.pao.group

So lets compare OWCP to RSII....

1- market valuation OWCP $325M $2.19 pps vs RSII $3M .0135 pps
2- OWCP- make take years and cost millions of dollars to do studies to submit a product to the FDA for approval...and only 10% ever get approved....VS RSII- will have precise forms of med cannabis ingredients to be compound and dispensed in different forms as soon as they start which is very soon. No studies required...Cash requirements minimal, Revs immediate.
3- OWCP Float about 150M vs. RSII 225M

"Our team has met with business operators that have real experience and expertise in multiple states and several business verticals within the cannabis industry," commented Management. "The business focus will center on working with physicians and pharmacists groups on the Research and Development of new, cutting edge treatments within the medical cannabis industry. Shareholders are encouraged to stay tuned to upcoming press releases and social media updates, where a detailed plan for RSII's entrance into this sector will be outlined."

Look & Listen at the video on Facebook with outside one of the labs of a compounding pharmacy: https://www.facebook.com/RisingIndiaUSA/?hc_ref=SEARCH&fref=nf

1- What is “compounding”?
In general, compounding is a practice in which a licensed pharmacist, a licensed physician, or, in the case of an outsourcing facility, a person under the supervision of a licensed pharmacist, combines, mixes, or alters ingredients of a drug to create a medication tailored to the needs of an individual patient.

2-Why do some patients need compounded drugs?
Sometimes, the health needs of a patient cannot be met by an FDA-approved medication. For example: if a patient has an allergy and needs a medication to be made without a certain dye; or
if an elderly patient or a child can’t swallow a pill and needs a medicine in a liquid form that is not otherwise available.

3-Are compounded drugs approved by the FDA?
Compounded drugs are not FDA-approved. This means that FDA does not verify the safety, or effectiveness of compounded drugs. Consumers and health professionals rely on the drug approval process to ensure that drugs are safe and effective and made in accordance with Federal quality standards. Compounded drugs also lack an FDA finding of manufacturing quality before such drugs are marketed.
Generally, state boards of pharmacy will continue to have primary responsibility for the day-to-day oversight of state-licensed pharmacies that compound drugs in accordance with the conditions of section 503A of the FDCA, although FDA retains some authority over their operations. However, outsourcing facilities that register under section 503B are regulated by FDA and must comply with CGMP requirements and will be inspected by FDA according to a risk-based schedule.