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[e-drug] USTR pressure on German system of reference pricing


  • From: "Mike Palmedo" <mpalmedo@wcl.american.edu>
  • Date: Tue, 03 Jul 2007 11:19:08 -0400

E-DRUG: USTR pressure on German system of reference pricing
--------------------------------------------------------

Hello,

In USTR's 2007 National Trade Estimate Report on Foreign Trade Barriers
contains a reference to a dispute between the US and Germany over
reference pricing of pharmaceuticals (I've cut and pasted the paragraph
below). Does anybody on this list know where I can find more information
on this dispute? Including the legislation mentioned in the report? Any
pointers I could get will be appreciated. Thanks.

Mike

[snip]

As part of a broader health-care reform package, Germany introduced a
reference pricing scheme on generic and patented pharmaceuticals on
January 1, 2005. U.S. firms contend that they bear the brunt of
cost-containment by virtue of their dominance (25 percent) of the German
market. U.S. pharmaceutical companies note serious concerns about lack
of transparency and fairness in the decisionmaking process related to
the new reference pricing scheme, which does not provide a fair rate of
return for patented, innovative medicines. Additional cost constraint
measures were imposed through the combining of patented, innovative
products with generic products, known as "jumbo groups." Both reference
pricing and its variant, jumbo groups, are strongly opposed by U.S.
pharmaceutical companies. The U.S. Government has raised this issue
repeatedly with the German government, including during the visits of
interagency U.S. health policy delegations to Berlin in June 2005 and
February 2006. Legislation that went into effect in May 2006 clarified
how drugs are declared innovative and provided more transparency in the
decision-making process, addressing some industry concerns. The German
government has continued to debate new, broader healthcare reform
legislation, but the packages put forward to date have not contained
further measures that would alleviate the disadvantages to U.S. and
other countries’ producers of innovative pharmaceuticals.

[snip]

--
Mike Palmedo
Research Coordinator
Program on Information Justice and Intellectual Property
American University, Washington College of Law
4910 Massachutsetts Ave., NW Washington, DC 20016
T - 202-274-4442 | F 202-274-0659
mpalmedo@wcl.american.edu