India and China: Outsourcing Beyond the Comfort Zone
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India and China: Outsourcing Beyond the Comfort Zone (continued)
The benefits: time and money
Why push the outsourcing envelope? Although cost-cutting often is the
first reason cited—and certainly a key concern—global outsourcing
can yield various benefits. First, time is money, and outsourcing can
save time. If companies can shorten today's long lead times for drug
development by handing off tasks to third parties that can perform them
more quickly because of fewer constraints or additional resources, they
will find themselves in an advantageous position. For example,
companies conducting clinical trials in India and China can take
advantage of a large population base and a diverse pool of currently
untreated patients, which are two factors that can accelerate clinical
trials.
Global and domestic outsourcing can play a key role in shortening the
drug development process by enabling pharmaceutical companies to hand
off selected tasks, thereby freeing up resources to devote more time to
additional strategic activities. Global outsourcing also can enhance
the quality of and access to talent. Many firms are tapping into
India's pool of scientists, who have solid capabilities and strong
expertise. AstraZeneca, for example, recently built a research facility
in Bangalore that focuses on tuberculosis. The company plans to invest
another US$30 million during the next five years for laboratory
equipment and operations costs. "Our investment here in Bangalore is
definitely not based on cost, because the cost of doing research is
mainly a small part of the total global research and development
efforts," Sir Tom McKillop, AstraZeneca's chief executive, told
India-based pharma portal pharmabiz.com. "The only reason for opting
for India is the quality of scientists."
Of course, the savings are compelling. The costs of direct and indirect
personnel, depreciation costs, and material are roughly 40% lower in
countries such as China and India (see Figure 2). Our analysis assumes
that indirect staff includes both local offshore and US corporate
oversight; local offshore oversight helps lower costs.
One example is clinical trial costs. ClinTec International, a privately
owned full-service contract research organization with headquarters in
Germany, for example, reports that recruiting 200 patients in the
United States for a one-year study would take approximately 3–6
months. ClinTec claims this time can be cut in half by recruiting
patients in India. The time required for data analysis also can be
significantly shorter, from 6–10 weeks in India versus nearly four
months in the United States. According to the company, the estimated
cost savings may reach 50–60% compared with the costs of conducting
the trials in the United States. Lower costs are a result of lower
wages of key personnel involved in conducting clinical trials and data
monitoring (e.g., clinical research assistants, project management,
clinical data management, and biostatisticians) and lower investigator
grants (i.e., payments to physicians for their expertise and time in
monitoring clinical-trial patients).
In addition to these savings, companies can avoid significant fixed
costs and capital outlays. For instance, by partnering with a local
pharmaceutical company for selected drug discovery efforts, companies
can minimize capital investment associated with setting up their own
R&D facilities in offshore locations. For labor-intensive
activities, the low costs of labor and infrastructure abroad are more
than enough to offset such added expenses as additional travel and
higher telecommunications costs. (continued)