BRIGHT GREEN CORPORATION GAINS MOMENTUM FOR THEIR “DRUGS MADE IN AMERICA” PLATFORM WITH APPROVAL FOR THE RESEARCH, PRODUCTION AND MANUFACTURING OF ALL SCHEDULE I AND SCHEDULE II PLANT-BASED DRUGS
22 Febbraio 2024 - 7:30PM
Bright Green Corporation (Nasdaq: BGXX) (“Bright Green” or the
“Company”) company announced today that final approval has been
received from the New Mexico Board of Pharmacy and the DEA for
unique licensing that allows Bright Green to register, license, and
authorize Schedule I and Schedule II plant-based drugs and Active
Pharmaceutical Ingredients (APIs) for research, production, and
manufacturing purposes. Schedule I Substances include Psilocybin,
psilocybin, mescaline, peyote, ibogaine Schedule II Substances:
Opium, poppy straw, raw opium, opium extracts, powdered opium,
granulated opium, tincture of opium, opium fluid extracts, opium
straw concentrates, pending: erythroxylon coca (cocaine)
Building on previous regulatory milestones like
DEA registration for Cannabis, Bright Green was able to
successfully navigate the uncharted territory of introducing
additional controlled substances, even amidst high levels of
uncertainty and complex pending policy changes at the federal
level. Achieving this substantial approval allows Bright Green to
bring their deep expertise to these issues to help propel our Drugs
Made in America movement forward. The company believes this effort
will help address the supply chain shortage for plant-based
medicines while establishing Bright Green Corporation as the
frontrunner for a share of the well-established assessable market
in the U.S. worth billions that is currently served extensively by
imports.
The research will be conducted the Company’s C2
team in Albuquerque, New Mexico, and the reshoring of production
and manufacturing to the U.S. will take place at the company’s
Grants, New Mexico facility. Medical plants will be produced in
climate-controlled glass greenhouses engineered to ensure quality
and predictability, laying a roadmap for guaranteed supply
contracts with both federal government entities and other
pharmaceutical interests. Bright Green expects to be the first
company in almost 100 years to produce, manufacture and supply API
for Schedule I and Schedule II controlled substances and to deliver
on contracts of this type.
“As we undergo an expansion of our
infrastructure, we plan to leverage the capital to be raised from
our exclusive EB-5 partnership with Asia Capital Pioneers Group, as
well as funding from federal agencies”, said Groovy Singh, CEO of
Bright Green. “The modular design of our facilities positions us to
scale with demand and ensure that as production grows, so does our
capacity to create jobs in direct correlation with EB-5 capital
availability in a methodical phased approach.”
Read more about the current state of pharmaceutical imports to
the U.S. here.
About Bright Green
Bright Green is one of the very few companies
selected by the US government to grow, manufacture, and sell,
legally under federal and state laws, cannabis and cannabis-related
products for research, pharmaceutical applications and affiliated
export. Our approval based on already agreed terms from the U.S.
Drug Enforcement Administration gives us the opportunity to advance
our vision of improving quality of life through the opportunities
presented by cannabis-derived therapies. To learn more,
visit www.brightgreen.us.
Cautionary Note Regarding
Forward-Looking Statements
This press release contains “forward-looking
statements” within the meaning of the “safe harbor” provisions of
the Private Securities Litigation Reform Act of 1995. These
forward-looking statements are made as of the date they were first
issued and were based on current expectations, estimates, forecasts
and projections as well as the beliefs and assumptions of
management as of such date. Words such as “expect,” “anticipate,”
“should,” “believe,” “hope,” “target,” “project,” “goals,”
“estimate,” “potential,” “predict,” “may,” “will,” “might,”
“could,” “intend,” “shall” and variations of these terms or the
negative of these terms and similar expressions are intended to
identify these forward-looking statements. Forward-looking
statements are subject to a number of risks and uncertainties, many
of which involve factors or circumstances that are beyond the
Company’s control. Such forward looking statements include, but are
not limited to, the ability of the Company to raise funds under the
Company’s EB-5 program, the impact that new officers, directors and
employees may have on the Company and the Company’s business and
results of operations, and the impact of the New Mexico Board of
Pharmacy and DEA approvals. The Company’s actual results could
differ materially from those stated or implied in forward-looking
statements due to a number of factors, including but not limited
to, risks detailed in the Company’s Annual Report on Form 10-K and
Quarterly Report on Form 10-Q, as amended and supplemented, as well
as other documents that may be filed by the Company from time to
time with the SEC. The forward-looking statements included in this
press release represent the Company’s views as of the date of this
press release. The Company anticipates that subsequent events and
developments will cause its views to change. The Company undertakes
no intention or obligation to update or revise any forward-looking
statements, whether as a result of new information, future events
or otherwise. These forward-looking statements should not be relied
upon as representing the Company’s views as of any date subsequent
to the date of this press release. Additional information regarding
these and other factors that could affect the Company’s results is
included in the Company’s SEC filings, which may be obtained by
visiting the SEC's website at www.sec.gov.
Media Contacts: Interdependence Public Relations
Owen Phillips /
Grace Connor
BrightGreen@Interdependence.com(310) 745-1407
Media Inquiries & Investor Relations
Contactir@brightgreen.us
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