THE US Food and Drug
Administration has revealed a
US$25m plan to be run over the
next 12 months to update its
prescription drug, device and food
safety review tools, under its
Regulatory Science Initiative.
The plan will see the agency
collaborate with industry pundits,
the government, scientists and
members of the academia to
improve its scientific standards,
which will in turn expedite
regulatory approval of new medicines.
Programs under the plan will
include research into potential
drug side effects using a patient’s
genetic code rather than animal
testing.The above article was sent to subscribers in Pharmacy Daily's issue from 07 Oct 10 To see the full newsletter, see the embedded issue below or CLICK HERE to download Pharmacy Daily from 07 Oct 10
IN WESTERN Australia, Michael’s Chemist Group has started stocking therapeutic Nicotine Vaping Products (NVPs), pursuant to the Federal Government’s new vaping laws (PD 25 Mar).
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