Rafarma
Pharmaceuticals and St. Petersburg-based Pharmsynthez have opened discussions for
Joint Venture Production.
At
meetings initiated by Governor Oleg Korolev of Lipetsk, Management from Rafarma
and Pharmasynthez have agreed in principal to commence a 'joint venture
production plan', with the potential to substantially increase revenues for
both companies. The agreement is contingent upon a satisfactory technical audit
of Rafarma's facilities by Pharmasynthez to be conducted next month.
The
joint venture production plan calls for various Pharmasynthez pharmaceutical
products to be manufactured in Rafarma's facilities, almost doubling capacity
and expanding market share accordingly. The Ontological and Antibiotic products
to be produced currently have domestic revenues of approximately $250,000,000.
While Pharmasynthez has an existing market share of approximately 20%, the
joint venture production plan with Rafarma anticipates increasing market share
to 35% or more.
"Rafarma?s
state-of-the-art facility is a sought-after partner in the rapidly-growing
Russian pharmaceutical industry and our expanding portfolio of products
continues to draw attention from industry participants and investors alike?
stated Rafarma CEO Dave Anderson.
About Rafarma
Pharmaceuticals, Inc.
Operating from a
new 270,000 square-foot state-of-the-art manufacturing and distribution
facility in Russia, Rafarma Pharmaceuticals produces generic antibiotics and
specialty pharmaceuticals in addition to its own line of proprietary products
that are approved by the Ministry of Health of Russian Federation. For the last
three years, the Russian Government has been highly focused on bolstering the
development of the nation's domestic pharmaceutical industry. Rafarma's mission
is to work under the auspices of these aggressive federal initiatives to
fast-track the modernization of Russia's pharmaceutical industry.
For more
information on Rafarma Pharmaceuticals, visit: http://rafarma.com
About
Pharmasynthez
Founded in 1996,
Pharmasynthez became a fully operational research and production facility in
2001 and currently conforming to GMP and GOST R 52249-2004 standards of
pharmaceutical manufacture and quality control. Pharmsynthez currently produces
Neovir?, Segidrin?, Fenasid? and
Penkrofton? used in oncology, gynecology, treatment of immunodeficiencies and
tuberculosis.
For more information
on Pharmsynthez, visit: http://en.pharmsynthez.com/Pharmsynthez.3.html
Safe Harbor Statement
Matters
discussed in this press release contain forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995. When used in
this press release, the words "anticipate," "believe,"
"estimate," "may," "intend," "expect"
and similar expressions identify such forward-looking statements. Actual
results, performance or achievements could differ materially from those
contemplated, expressed or implied by the forward-looking statements contained
herein. These forward-looking statements are based largely on the expectations
of the Company and are subject to a number of risks and uncertainties. These
include, but are not limited to: the impact of economic, competitive and other
factors affecting the Company and its operations, markets, product, and
distributor performance.
RELATED LINKS
Website:
www.Rafarma.com
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SOURCE Rafarma
Pharmaceuticals, Inc. (RAFA)