Pharmaceutical policy is the role that government plays in
determining the rate at which new drugs are developed, what drugs are
developed, who has access to the drugs that are developed, and the
choice of drugs by doctors and their patients. The goal of
pharmaceutical policy is to provide the maximum benefit to health for
whatever amount is spent on pharmaceuticals. A good policy in any
area of health care will produce the most health at the least cost.
This first premise, although it may be new to some of you, is a
generally accepted premise of public policy analysis: more of a good
thing is better than less (whether it be educational levels, health,
or economic production) and getting more of a good thing at the least
cost is better, as that leaves the surplus to be allocated to
obtaining more of other good things (so getting more health for less
dollars would allow us to spend more on schools, for example).
The
United States, as in most countries in the developed world, does not
have a central government agency entrusted with determining
pharmaceutical policy and allocating funds to drug development and
drug distribution. Most of the drugs that are prescribed in the
United States, as well as in other countries, are developed by
for-profit pharmaceutical companies that operate in response to
market forces. However, the marketplace in which those companies
operate is an extraordinarily complex one, with substantial
regulation and extraordinary information costs- the well-known high
cost of the clinical trials for drug approval is just one example of
the expense of generating essential high quality information about a
drug. Pharmaceutical policy is the product of a number of areas of
law and regulation that all have an effect on drug development and
drug usage in the context of this complex market for drugs starting
with the NIH's role in basic research, and includes patents, FDA
approval, our patchwork pharmaceutical benefit coverage, the First
Amendment's protection for pharmaceutical companies commercial
speech, and product liability. The purpose of this blog is to discuss
and examine developments in all the areas of law and regulation that
impact drug development, access, and consumption.
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