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INDIA
TO SET UP CENTRALISED DRUG LICENSING AUTHORITY
By Prashant K. Nanda, New Delhi, October 7, 2007 (IANS)
Concerned
over the rampant spread of spurious medicines in India, the government
is planning to disallow states from issuing licences to drug companies
and to set up a federal authority instead on the lines of the US
Food and Drugs Administration (FDA).
"Currently,
both the centre and the state governments are empowered to issue
licences for the manufacturing of drugs. But this will change in
the near future," Health Secretary Naresh Dayal said.
"Unfortunately,
the control mechanism of state regulating bodies is not efficient.
And their inefficiency is one of the key factors why spurious drugs
are flourishing in the country. We will withdraw the drug-licensing
power from them and start a centralised licensing system,"
Dayal told IANS.
The
secretary said the centre has moved a bill to form a central drug
authority and it has been referred to the standing committee.
The
new body will be fully autonomous and be modelled on the lines of
the FDA in the US. It will have 10 sections like a clinical trial
division, biotech division and pharmaco vigilance division.
"We
are quite hopeful that by the coming budget session we will have
the power to do so. The process of withdrawing licensing powers
from states will start thereafter," he said.
"The
central drug authority will follow the Good Manufacturing Practice
(GMP) norms set by the World Health Organisation (WHO) and thus
give India a better name in the field of drug export."
He
said recently India had signed an agreement with the Philippines.
"Our drug market is growing and the Philippines Friday signed
an agreement with us to make India a source for importing medicines."
"Medicine
costs there are too high and nearly 40 percent of the population
is below the poverty line. They want to take advantage of our low
cost medicine. When the global community is looking towards us,
we should make our vigilance mechanism stronger," Dayal added.
He
said his ministry is going to fill up many vacancies of drug inspectors
and this will help the cause of surveillance.
Dayal
said the Drugs and Cosmetics Act will be amended in the near future
to put a high penalty on spurious drug manufacturers and those involved
in their marketing.
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