THE US FDA has issued warnings
to Pfizer over its lax monitoring of
physicians who are testing
experimental drugs on patients.
The problem stems from ongoing
testing of its new bipolar drug,
Geodon, of which 12 people have
so far suffered from overdoses.
According to reports, the FDA
has cracked down on Pfizer after it
found the company was not
following its own guidelines for
safely conducting the study, and
was not alerting investigators to
dosing problems as they occurred.The above article was sent to subscribers in Pharmacy Daily's issue from 21 Apr 10 To see the full newsletter, see the embedded issue below or CLICK HERE to download Pharmacy Daily from 21 Apr 10
MAYNE Pharma Group Limited has filed a patent infringement suit against Sun Pharmaceutical Industries Ltd and Inc., in the United States District Court, according to yesterday’s ASX announcement.
PHARMACY Connect 2024 conference will feature a provocative ‘Great Debate’ during the Harm Minimisation Workshop on Thu 05 Sep at the Hyatt Regency in Sydney.
LTR Pharma Limited has successfully raised $10.5 million through a share placement to sophisticated and new institutional investors, significantly surpassing initial demand.
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