[e-drug] Time needed to provide bioequivalence studies

e-drug
1

E-drug: Time needed to provide bioequivalence studies
-------------------------------------------------------------------------

I would appreciate information on the amount of time that is
normally required for generic companies to conduct and organize
the various bioequivalence studies required for drug registration in
Europe, the United States, Canada, Australia or South Africa.

Jamie

James Love
Consumer Project on Technology
http://www.cptech.org
1.202.380.3080 fax 1.202.234.5176
mailto:love@cptech.org

--
Send mail for the `E-Drug' conference to `e-drug@usa.healthnet.org'.
Information and archive http://satellife.healthnet.org/programs/edrug.html
Mail administrative requests to `majordomo@usa.healthnet.org'.
For additional assistance, send mail to: `owner-e-drug@usa.healthnet.org'.