1.
My topic is on the involvement of the FDA in
regulating the development of pharmaceutical drugs, in particular compounding pharmacies.
2.
There is always a debate about how much the
federal government should regulate businesses. The manufacturing and production
of drugs is no different. Should the FDA regulate compounding pharmacies’ and pharmaceutical
companies more or less? Especially with the recent outbreak of meningitis
derived from a contaminated product produced at New England compounding pharmacy,
there are concerns about the lack of FDA regulation.
3.
I can find references in the Napa City County
Library and find numerous apt articles on the internet involving the recent meningitis
outbreak and the role of the FDA in the approval a drugs.
4.
Everyone is concerned about their health and it
is particularly disturbing when doctors and known medicines, which are entrusted
to help individuals, are the cause of illnesses. People are continually trying
to improve their health and minimize risks associated with ingesting unknown
compounds.
5.
The role of the FDA involvement in business is
always questioned. It is an ongoing debate that was catalyzed by Upton Sinclair’s
The Jungle. The meningitis outbreak
is relatively new so I doubt that many AP students have already written papers
involving that particular event.
6.
Should I narrow my topic and just talk about
compounding pharmacies’ regulations or expand my subject area so that my paper
discusses pharmaceutical companies’ regulations?
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