Jim
Miller is the president of PharmSource Information Services,
Inc., and
publisher of Bio/Pharmaceutical Outsourcing Report, tel. 703.914.1203,
fax 703.914.1205, info@pharmsource.com,
www.pharmsource.com
At
a widely anticipated and closely scrutinized presentation
to analysts in April, Pfizer announced that it will cut $4 billion out
of its cost structure during the next four years. The company said the
restructuring is required in the face of an anticipated revenue
weakness resulting from the loss of patent protection for several key
drugs, plus the decreased performance of its COX-2 inhibitors, Celebrex
and Bextra. The announcement was preceded two days earlier by the
withdrawal of Bextra from the market at the insistence of FDA.
The size of the cost cuts was nearly double what Wall Street
analysts had been expecting, but the company provided few details to
analysts or its employees regarding where the cost reductions would
come from. More insight came the next day at this year’s “Partnerships
with CROs” conference in Dallas, where Pfizer’s
(New York, NY, www.pfizer.com)
Chief Finance
Officer Alan Levin talked about efforts
the company is making to rein in R&D expenses.
Levin said that in Pfizer’s new CRO selection paradigm,
competition is the norm and price is an explicitly considered and
heavily weighted factor. Quality, which traditionally was a key
decision criterion in CRO selection, is now the price of entry into the
vendor pool. In other words, a CRO is allowed to submit a proposal only
if its quality is acceptable. Competition among accepted vendors is
used to drive down prices, with the help of e-procurement tools such as
online reverse auctions (a real-time bidding process in which vendors
compete by besting each other’s posted price). Levin also said that
Pfizer is turning increasingly to offshore locations such as India and
China to source R&D services and conduct studies.
Mark J. Guinan, CFO for Johnson &
Johnson’s (New
Brunswick, NJ, www.jnj.com) R&D
operations, copresented with Levin
and emphasized the theme of competition. Guinan announced that Johnson
& Johnson has established a central services group to support
clinical trial activities for the company’s constituent R&D
operations, including Johnson & Johnson, Alza, Centocor, and Scios.
The central services group will bid against CROs to provide services
for the company’s clinical studies. The goal, said Guinan, is to drive
down costs while increasing the quality of services provided.
Wyeth
(Madison, NJ, www.wyeth.com)
representatives told the conference
about the company’s latest effort to control costs—a strategic sourcing
deal with RPS to provide field monitoring staff. This is the second
year in a row in which Wyeth has showcased an innovative approach to
outsourcing. This past year, company representatives described an
initiative to outsource all clinical data management activities to
Accenture. According to the company’s presentation, that initiative has
been very successful at lowering data management costs.
Big Pharma’s admission that it is making decisions on the
basis of price should be a wake-up call to the entire contract services
industry, including contract manufacturers. For a long time,
contractors have convinced themselves that quality (among other
factors) trumped price as a decision criterion. Now major
pharmaceutical companies are saying that quality and compliance are
necessary for doing business with them, but not sufficient.
Of course, price is not the same as cost. Wyeth’s efforts
with Accenture
(www.accenture.com)
and Research
Pharmaceutical Services
(Plymouth Meeting, PA, www.rpsweb.com)
are a recognition that
operational efficiency, combined with an appropriate level of
offshoring, may deliver significant cost savings. The concern for the
industry should be that the focus on price will drive out truly
cost-saving innovations. (continued)