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Please note the legal information at the beginning of the presentation. Version A
Disclaimer
General information:
By making use of this document the reader acknowledges and agrees to the following: We accept no liability arising from the use of this
document. STADA Arzneimittel AG, Bad Vilbel (in the following “STADA”), has made every effort to make sure that this document contains
correct and up-to-date information. However, it accepts no responsibility or guarantee whatsoever in respect of topicality, accuracy and
completeness of the information and assumes no obligation to update, complete or correct the information contained therein. The anticipated
opportunities and risks to STADA’s activities have been described in detail in the Executive Board’s management reports in the annual reports.
Current possible opportunities and risks are mentioned in the respective interim report. STADA’s performance indicators are party influenced by
one-time special effects and/or effects not arising from the operating business. Disclosure of key figures adjusted for these effects (so called
“pro forma” key figures) by STADA is only to provide a supplement to the recorded IFRS key figures for a transparent comparison to a relevant
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This document may not be reproduced in whole or in part without the express written consent of STADA. Any disputes arising out of or in
connection with the content of this document, insofar as they are directed against STADA, shall be subject to German law, without prejudice to
mandatory provisions of foreign law. The place of jurisdiction is Frankfurt am Main to the extent legally permissible .
Forward-looking statements:
This STADA Arzneimittel AG presentation (subsequently "STADA") contains certain statements regarding future events (as understood in the
U.S. Private Securities Litigation Reform Act of 1995) that express the beliefs and expectations of management. Such statements are based on
current expectations, estimates and forecasts on the part of company management and imply various known and unknown risks and
uncertainties, which may result in actual earnings, the financial situation, growth or performance to be materially different from the estimates
expressed or implied in the forward-looking statements. Statements with respect to the future are characterized by the use of words such as
“expect”, “intend”, “plan”, “anticipate”, “believe”, “estimate” and similar terms. STADA is of the opinion that the expectations reflected in forward-
looking statements are appropriate; however, it cannot guarantee that these expectations will actually materialize. Risk factors include in
particular: The influence of regulation of the pharmaceutical industry; the difficulty in making predictions concerning approvals by the regulatory
authorities and other supervisory agencies; the regulatory environment and changes in the health-care policy and in the health care system of
various countries; acceptance of and demand for new drugs and new therapies; the influence of competitive products and prices; the availability
and costs of the active ingredients used in the production of pharmaceutical products; uncertainty concerning market acceptance when
innovative products are introduced, presently being sold or under development; the effect of changes in the customer structure; dependence on
strategic alliances; exchange rate and interest rate fluctuations, operating results, as well as other factors detailed in the annual reports and in
other Company statements. STADA not assume any obligation to update these forward-looking statements or adapt them to future events and
developments.
Please note the legal information at the beginning of the presentation. Version A
Milestones in the STADA history
1895 Founded in Dresden as a pharmacists'
cooperative
1970 Stock corporation with restricted
registered common shares only for
pharmacists
1975 Market entry in the starting generics
market
1986 Beginning of internationalization
1998 Starting trading at the stock exchange
2001 Included in MDAX on July 23, 2001
2004 Start in Eastern Europe: Acquisition of
Nizhpharm, Russia
2006 Expansion in Eastern Europe:
Acquisition of Hemofarm Group, Serbia
2010 As of Sept. 30, 2010
Enterprise value1): € 2.1 billion
Employees: approx. 8,000
Shareholder structure: approx. 14%
pharmacists and doctors
€ 879.1 million.
Please note the legal information at the beginning of the presentation. Version A
Roadmap
2009 2014
Organic Group development Group sales: approx. € 1.57 Group sales: approx. € 2.15
based on proven success factors:
billion billion
EBITDA: approx. € 280 million EBITDA: approx. € 430 million
Positioned in growth markets
Net income: approx. € 100 million Net income: approx. € 215 million
Strong product development
Assumptions/framework
+
Broad international sales
Investments BtF until 2013
infrastructure
+
„STADA approx. € 20 million
Continuous cost optimization
„STADA ––
build
build the
the future“
future“ Expenses BtF (one-time special
Cautious acquisition policy (BtF) effects) until 2013 approx. € 50
(BtF) until 2013
bis 2013
million
Forecast range +/- 5%
1) IMS MIDAS Dec. 2009; IMS Generic Market Prognosis, June 2009; IMS Thought Leadership analysis prepared for STADA, Dec. 2009.
2) IMS Generic Market Prognosis, June 2009; IMS Thought Leadership analysis prepared for STADA, Dec. 2009. The market data on generics fluctuate (in some
cases substantially) due to differing market definitions from source to source.
3) Business risks and consequences of the global financial and economic crisis are described in detail in the annual report 2009, particularly in the risk report.
230 261
242
203 235
227
179 211 206
159 184 185
168
122 131 156
137 153
93 128
105
89
86 86 RX Generics OTC
72
59
2005 2006 2007 2008 2009 2010 2011 2012 2013 2014
The Russian market has an estimated value TOTAL MARKET: 12.0% CAGR
of ruble 555 billion in 2010. Generics: 13.2% CAGR
Above average growth rates with 12% p.a. OTC: 9.6% CAGR
between 2010 and 2014 expected
RX: 12.8% CAGR
(in comparision 10.5% India, 11.9% China).
GER
1.3 Total volume Germany 2010-2013 (at current
1.1 1.0 prices and volumes):
0.7 > € 4 billion
Asien ~ 10%
Ho Chi Minh City (Vietnam; 50% JV)
Beijing (China; only locally)
Sites which outside of the EU have been oriented at least partly to the production of individual product for the EU or which have been approved by EU
authorities after local auditing.
MAKIZ
(Russia)
Hemofarm 1,646
(Serbia) 1,571 1,569
Nizhpharm
Crinos (Russia) 1,245
(Italy) Sales
Bayvit
1,022 growth
Clonmel (Spain)
814 adjusted1)
Healthcare
(Ireland)
745 2009: +4%
634
538
467
2000 2001 2002 2003 2004 2005 2006 2007 2008 2009
1) Adjusted for changes in the Group portfolio as well as from currency effects.
Acceleration of
Reduction of More efficient
continuous cost
complex Group centralized control
optimization
structures of Group
Focus: Cost of sales
companies
Production sites
Organizational structures
Personnal/reporting structures
3rd quarter
4th quarter
Since Oct. 1, 2010 new functional reporting lines & organizational structures
Foreign subsidiaries with direct reporting lines to the corporate headquarter.
More transparent and faster decision making processes
Further measures planned
Please note the legal information at the beginning of the presentation. Version A
Highlights 1-9/2010
1) Adjusted for one-time special effects as well as effects from currency influences and interest rate hedge transactions.
By segment By region
Core segments € 1,127.1 million Total Group € 1,177.8 million
+3%, (+2%) +3%, (+2%)
26.4% 22.9%
() = Adjusted for sales contributions from acquisitions and disposals as well as currency effects.
France 57.0 5% -3
Germany +(+) Health care reform 2011 with moderate upside potential
Expected
21.3
16.9 recovery of the
14.5
Serbian business
+12% +15%
-4% 224.2 165.6
200.4 -19%
143.5
190.2 182.9 129.1
104.9
Margin Margin
16.7% 15.5% 17.6% 19.0% 11.3% 8.9% 12.6% 14.1%
Underlying business clearly improved, adjusted operating margins expanded; reported operating
profit burdened by one-time special effects of € 60.7 million in 1-9/2010
1) Adjusted for one-time special effects as well as effects from currency influences and interest rate hedge transactions.
-0.7 Other
adjusted1) 165.6
1) Adjusted for one-time special effects as well as effects from currency influences and interest rate hedge transactions.
Equity and liabilities in € million Dec. 31, 2009 Sept. 30, 2010
A. Equity 869.7 837.0
B. Non-current liabilities and provisions 683.5 1,113.2
C. Current liabilities and provisions 898.5 481.2
Total equity and liabilities 2,451.7 2,431.4
Net debt in € million Net debt reduced by approx. € 126 million within one
year to € 879.1 million in 1-9/2010
1) Adjusted for one-time special effects as well as effects from currency influences and interest rate hedge transactions.
2) Linear extrapolation of the (adjusted) EBITDA 1-9/2010 on a full year basis.
Bond
Amounts due to banks
36.2 Promissory notes
51.8 350.0
244.0
195.5
24.1 10.8
9.6 35.0 11.0 50.5 22.1
2010 2011 2012 2013 2014 2015 > 2015
Issuance of a corporate bond on April 21, 2010 (€ 350 million nominal value, 4.0% p.a. bond due April
2015)
Maturity of the next bigger tranche of promissory notes in the amount of € 195.5 million in the fourth
quarter of 2011
Short-term liabilities to banks with maturity under one year: accepted credit lines which have been provided to
STADA by banks on a revolving basis for years
Weighted interest burden for Group financial liabilities on Sept. 30, 2010:
4.8% (Dec. 31, 2009: 3.8%); switch of a euro loan in Russia into ruble in order to minimize the currency risk
exposure of the Group
Total expenses 2007-2009 € million Total expenses 1-9/2010 vs. 1-9/2009 in € million
51.8 56.2
-14.0
-100.7 -140.6
-515.9
2005 2006 2007 2008 2009 1-9/2009 1-9/2010
1) Free cash flow includes cash flow from operating activities and cash flow from investing activities.
1) Adjusted for one-time special effects as well as effects from currency influences and interest rate hedge transactions.
Martina Cailloud
E-Mail: martina.cailloud@stada.de
Jessica Gepel
E-Mail: jessica.gepel@stada.de
Melanie Weis
E-Mail: melanie.weis@stada.de
Please note the legal information at the beginning of the presentation. Version A
Share capital and shareholder structure
1) Owners of the restricted registered common shares must be recorded in the shareholders’ register in order to be able to exercise their shareholders’ rights.
Recording in the shareholders’ register is only possible with the approval of the Executive Board.
2) The purchase of up to further 10% of the capital stock in own shares until Dec. 10, 2010 was approved by the shareholders’ meeting 2009.
3) Additional authorized capital of 29.4 mill. common shares.
4) Exercise price for subscription of 20 common shares: € 329.00.
Source: STADA estimate at ex-factory prices based on market data provided by various international market research institutes.
1) Share in percent of the generics capable market.
P&L effects due to foreign currency items for monetary assets & liabilities
Increase of cost of sales ratio, among other things, due to the deliberate avoidance of sales possible in order
to reduce the default risk on receivables and seasonal higher advertising costs
Tax rate 1-9/2010: 41.1% (1-9/2009: 21.8%); affected by shifts in regional earnings mix and limited tax
deductibility of one-time special effects
1) In financial year 2009, development expenses for new products in the amount of € 14.8 million were capitalized.
After taxes:
1-9/2010: -53.6 one-time special effects 1-9/2010 after taxes (netted); (1-9/2009: € -9.4 million)
thereof -14.1 burden as a result of expenses in connection with the „STADA – build the future“ project
After taxes:
1-9/2010: +1.2 non-operational earnings-influencing effects 1-9/2010 after taxes (netted);
(1-9/2009: € -3.4 million)
Residual carrying amounts of intangible assets at the end of reporting period in € million
Top position in terms of goodwill with unproblematic impairment test as at Sept. 30, 2010:
Hemofarm subgroup: € 107.1 million
Nizhpharm/MAKIZ (joint Cash Generating Unit): € 68.2 million
Additional > € 500 million of value in use alone for all consolidated companies with goodwill that, in
accordance with IFRS, cannot be reported in the balance sheet (by making use of the criteria for
impairment testing that are usual at STADA)