Project Summary Documents
Project Summary Documents (PSDs) are disclosed for each project prior to Board
consideration. They contain project descriptions, financial details, client
information, environmental issues, tender guidelines, and contact details.
PSDs for private sector projects are disclosed at least 30 days prior to Board
consideration and for state sector projects, at least 60 days.
Project Summary Documents
Signed projects
Board approval is the final stage in the project approval process. After Board
approval, the EBRD and the client sign the deal and it becomes legally
binding. Signed project lists reflect year-end data.
Signed projects
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Case studies
Nizhpharm, pharmaceutical manufacturer, Russia
In 1998 Nizhpharm, a Russian producer of ointments, creams and suppositories,
received a US$10m investment from Quadriga-managed St Petersburg and Central
Russia RVF and Lower Volga RVF.
Like many Russian pharmaceutical manufacturers, Nizhpharm's product portfolio
consisted of a number of established medications but lacked innovative generic
pharmaceuticals, which could boost the company's growth.
The investment was used to acquire modern equipment and refurbish the
production facilities according to the stringent European requirements which
ultimately allowed full GMP certification, enabling the company to become the
first Russian GMP-certified drug manufacture.
The new management has focused on four therapeutical classes and updated its
portfolio with high marginal branded generics and the range of products by
40%.
Own sourcing of new products from the company’s R&D centre was enhanced and
supported with licensing of advanced drugs from foreign partners. Both sources
have significantly strengthened the company’s growth potential. As a result ,
Nizhpharm’s portfolio is currently composed of 70% branded, promoted products
and 30% high margin non-promoted drugs. The company enjoys one of the fastest
new product-to-market introduction periods in the industry.
The reorganisation of the company's sales force has supported the introduction
of the new product line and allowed expansion into neighbouring countries,
such as Ukraine and Kazakhstan.
Quadriga, together with the other key shareholders, have worked diligently
over the previous five years to establish Nizhpharm as a leading branded and
generic pharmaceutical producer in Russia with an average sale growth of 33%.
The combination of a top quality GMP certified production facility in Nizhny
Novgorod and a comprehensive national medical representative and merchandising
team, has ensured strong sales growth and excellent profitability margins.
This, coupled with an excellent history of 100% accounting transparency and
solid corporate governance principles, has enabled Nizhpharm to become one of
the most praised assets of Russian pharmaceutical market.
Saw Mill, Arkhangelsk, Russia
In 1996 EBRD and Norum (Cyprus) Ltd invested $2 million into Saw Mill No.3 in
Arkhangelsk, acquiring a 30% stake. The company was loss-making. The
investments installed a new boiler station enabling the company to shift from
heavy fuel oil to forestry waste dry the end sawn good products. Other new
equipment improved performance and quality.
Output tripled over the next 5 years. Using increased cash-flow, the company
introduced new technologies and continued its reconstruction while most other
saw mills faced severe production problems and decreasing output. The Fund
Manager developed production technology, restructured organisation and
ownership and encouraged better financial administration and regular
reporting. Today, output capacity is 150,000 m3 and the company exports 80% to
western Europe.
In 2002, the EBRD, Norum (Cyprus) Ltd and several other shareholders sold
their majority stake to a strategic Russian investor on attractive terms. The
saw mill's profitability, professional management, transparency, long audit
history and clear development plan were key factors for investors.
Supporting the Polish pharmaceutical industry
Polfa Kutno S.A. was established in 1935 and has become one of Poland’s
leading pharmaceutical companies. Following privatisation in 1995, the EBRD
acquired a controlling stake via its participation in the Polish Private
Equity Funds I and II and in conjunction with the Polish American Enterprise
Fund.
Over the next 7 years, a restructuring process was implemented which focussed
on new product development and quality improvement. This process involved
divestment of non-core activities, recruitment of new CEO, CFO and Commercial
Director, increased focus on high margin new products, development of 145 rep
offices and construction of a modern production facility with EU Good
Manufacturing Practices. As a result, Polfa Kutna received the GMP certificate
confirming its compliance with the highest standard for product manufacturing
and control.
The funds sold their stakes in 2003 to Polish pension funds at a cost multiple
of 5.4x. In 2004, following profits of USD 8 million, Polfa Kutna made a
public offer for the State Treasury’s 29.84% stake in another pharma
manufacturer, Jelfa, and is spearheading consolidation of Poland’s healthcare
sector.