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Forest David
A. Case Abstract
Bristol Meyers Squibb (BMY) is a comprehensive strategic management case that includes the company’s
year-end 2010 financial statements, organizational chart, competitor information and more. The case time
setting is the year 2011. Sufficient internal and external data are provided to enable students to evaluate
current strategies and recommend a three-year strategic plan for the company. Headquartered in New
York, New York, BMY’s common stock is publicly traded under the ticker symbol BMY.
Headquartered in New York City, Bristol-Myers Squibb is a huge pharmaceutical firm with such
blockbuster cardiovascular drugs as Plavix and Avapro for hypertension. BMY also produces antipsychotic
medication Abilify and HIV treatments Reyataz and Sustiva. BMY also has excellent products
in immunoscience, metabolics, neuroscience, oncology, and virology. BMY has 12 manufacturing
plants worldwide and conducts research and development in four countries, sells its products globally; the
US accounts for two thirds of BMY’s sales.
1. Customers
2. Products or services
3. Markets
4. Technology
5. Concern for survival, growth, and profitability
6. Philosophy
7. Self-concept
8. Concern for public image
9. Concern for employees
Threats
1. The two provisions of the US health care over haul: 1) an annual fee on pharmaceutical companies,
and 2) new discounts for Medicare patients who hit the prescription coverage gap.
2. In May 2012, BMY patent protection on Plavix expires.
3. Bloomberg’s Business Week warned BMY has financial challenges ahead in 2012 and downgraded the
stock to “hold” from “buy.”
4. For every 5,000 compounds discovered only one reaches the pharmacist’s shelf.
5. Less than 1/3 of all marketed drugs achieve enough commercial success to recoup their R&D
investments.
6. With regulations it can take 12 to 15 years from time patent is received until the drug hits the market.
7. Many competitors in the market with Pfizer being the largest yet only having 8% of the market.
8. Patent infringement in developing countries not honoring patents from other nations.
9. FDA requires 3 phases of expensive human testing before a drug can be approved.
Bristol Meyers
Pfizer Merck
Squibb
Critical Success Factors Weight Rating Score Rating Score Rating Score
Advertising 0.05 2 0.10 4 0.20 3 0.15
Market Penetration 0.12 2 0.24 4 0.48 3 0.36
Sales 0.15 2 0.30 4 0.60 3 0.45
Product Quality 0.15 2 0.30 4 0.60 3 0.45
R&D 0.12 2 0.24 4 0.48 3 0.36
Products Offered 0.10 2 0.20 4 0.40 3 0.30
Financial Profit 0.16 2 0.32 4 0.64 3 0.48
Market Share 0.15 2 0.30 4 0.60 3 0.45
Totals 1.00 2.00 4.00 3.00
E. Internal Audit
Strengths
Liquidity Ratios
Debt/Equity Ratio 0.34 1.03 1.00
Current Ratio 2.0 0.8 1.3
Quick Ratio 1.8 0.7 0.9
Profitability Ratios
Return On Equity 20.5 30.0 26.0
Return On Assets 15.2 8.8 8.9
Return On Capital 19.3 11.4 11.8
Return On Equity (5-Year Avg.) 18.8 22.9 23.8
Return On Assets (5-Year Avg.) 11.5 10.3 8.0
Return On Capital (5-Year Avg.) 15.3 13.8 10.8
Efficiency Ratios
Income/Employee 180,407 90,604 126,905
Revenue/Employee 774,111 652,532 1 Mil
Receivable Turnover 10.1 5.6 15.4
Inventory Turnover 4.1 2.7 12.5
F. SWOT
SO Strategies
WO Strategies
1. Increase R&D by $200M for the production of specialty drugs (W1, W2, O2, O4).
2. Produce drugs losing their patents status in Japan and Europe (W4, O6).
ST Strategies
1. Initiate a $200M advertising campaign to market new drugs before they hit the market (S7, T2).
2. Start production of generic OTC drugs (S1, T6).
WT Strategies
1. Add a division for the production of OTC drugs for $200M (W4, T6).
FP
Conservative Aggressive
7
CP IP
-7 -6 -5 -4 -3 -2 -1 1 2 3 4 5 6 7
-1
-2
-3
-4
-5
-6
-7
Defensive Competitive
SP
Quadrant II Quadrant I
BMY
Weak Strong
Competitive Competitive
Position Position
High
3.0 IV V VI
The
EFE
Total Medium BMY
Weighted
Scores
Low
1.0
Add division
Add 2 plants for OTC
drugs
Opportunities Weight AS TAS AS TAS
1. FDA approval for BMY drug Yervoy to fight melanoma. 0.09 3 0.27 1 0.09
2. Global pharmaceutical sales are expected to expand up to 7
0.09 3 0.27 2 0.18
percent over 2011.
3. Pfizer’s Lipitor and Lilly’s Zyprexa patents expire in 2011. 0.09 2 0.18 3 0.27
4. Specialty drugs have accounted for close to 2/3 of all new drugs 0.05 4 0.20 1 0.05
5. launched.
The industry has some of the highest barriers to entry of any US 0.05 3 0.15 2 0.10
6. Generic drugs are only slightly less expensive than branded
0.04 4 0.16 2 0.08
ones in Japan and Europe.
7. FDA will often allow drugs to become OTC drugs as their patent
0.03 2 0.06 4 0.12
ends.
K. Recommendations
1. Add 2 new manufacturing plants in China for $200M.
2. Product generic versions of Lipitor and Zyprexa for $100M.
3. Increase R&D by $200M for the production of specialty drugs.
4. Add a division for the production of OTC drugs for $200M.
M. Epilogue
For Q3 of 2011, BMY reported a 2 percent increase in profit, as price increases and higher sales of most
key medicines were nearly offset by higher R&D and marketing spending. BMS’s net income in Q3 was
$969 million, or 56 cents per share, up from $949 million, or 55 cents per share, a year earlier, while the
company’s revenue rose 11 percent to $5.35 billion. The company did acknowledge though that two
provisions of the U.S. health care overhaul cut profit by about 4 cents a share in Q3. The two provisions
were: 1) an annual fee on pharmaceutical companies, and 2) new discounts for Medicare patients who hit
the prescription coverage gap. Despite these new laws, BMY at Q3 2011 raised the low end of its full 2011
EPS forecast from $2.25 to $2.30 per share.
As Q3 2011 ended, CEO Lambertville Andreotti told analysts that BMY made five important deals recently
that led to its second straight quarter with double-digit sales growth, a rarity in this industry. In September
2011, BMS bought Amira Pharmaceuticals, a developer of treatments for the fatal lung disease pulmonary
fibrosis and other disorders. During Q3, Bristol made deals with three other companies to develop new
drugs for cancer, diabetes and other diseases. BMY also secured a licensing deal to develop a once-a-day
HIV pill combining its Reyataz and a Gilead Sciences Inc. drug now in testing.
The Food and Drug Administration (FDA) recently pushed back its review deadline until January 2012 for
a much-anticipated new type of diabetes drug. In July 2011, the FDA advisers recommended against
approving dapagliflozin, a drug developed by BMS and partner AstraZeneca PLC. The ruling was due to
higher rates of bladder and breast cancer seen in patient testing. The Type 2 drug works by eliminating
excess blood sugar via urine.
For Q3 2011, BMY’s U.S. sales totaled $3.5 billion; foreign sales hit $1.9 billion. Sales were led by
Plavix, the world's second-best-selling drug, up 8 percent to $1.79 billion. Another BMY drug, Abilify, for
During Q3, BMY’s spending on marketing, sales and administration jumped 14 percent, to $1 billion,
partly because of costs to launch new products, including Yervoy. Research and development costs
increased 18 percent, to $973 million, mostly for expensive late-stage human testing.