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Online edition of India's National Newspaper Sunday, August 19, 2001 |
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Southern States
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Govt. decision on vaccine irks bio-tech company
By Our Staff Reporter
HYDERABAD, AUG. 18. The State Government's decision not to source
the Hepatitis B vaccine from ``local companies'' under the Bill
Gates-funded vaccination programme, has prompted city-based
Shantha Biotechnics to question its `sincerity' in promoting
biotechnology companies in the State.
Shantha Biotechnics, which makes the Shanvac B (Hepatitis B)
vaccine at its Medchal unit, was one of the three companies which
responded to the Government's call for tenders, the others being
Bharat Biotech (Hyderabad), and Panacea Biotech of Delhi.
However, following a controversy over the production process
adopted by one company, the State Government asked UNICEF to
procure vaccine from multinationals, because it was not sure of
the `local' quality.
Making a presentation on the company's plans and production
facility at its unit in Medchal on Saturday, Mr. K.I. Varaprasad
Reddy, Managing Director, Shantha Biotechnics, said the fact was
that Gates Foundation approached the Andhra Pradesh Government
for its maiden Hepatitis-B vaccination programme in India only
because the country's first r-DNA vaccine was developed in
Hyderabad by Shantha Biotechnics.
It was ironical that the State Government which claims that it
supports the biotech industry was trying to patronise foreign
companies for its very own requirement, he observed adding that
the company would make a representation to UNICEF on the basis of
the quality of their vaccine and production facility.
The Government, he said, took the decision on the pretext that
Indian companies do not have WHO approvals. However he pointed
out that even WHO clearly states that its approval was not
necessary for ``national purchases.'' Moreover all six vaccines
procured for the national immunisation programme are not WHO
approved (except for one or two from the Serum Institute).
Shantha Biotechnics already has other orders from UNICEF, for 3.3
million doses in 2002 and 5 million in 2003, with a
prequalification that they obtain WHO approval (international).
Mr. Reddy said WHO undertook an audit in the Shantha Biotechnics
unit in July for Current Good Manufacturing Practices (CGMP)
certification. It made some suggestions mainly in the areas of
layout (of infrastructure) and validation protocol. Another audit
will be done in December, and the company expects the approval.
Mr. Reddy was also critical of the Government Biotechnology
Policy. It was not enough to offer 50 acres (Biotech Park) or
give sales tax deferment, he said.What was needed was to have a
regulatory system to guide. There should be testing labs. The
Drug Controller should be upgraded to have microbiologists and
there should be incubation centres to take up training. The
sector needed customs duty exemption on biotechnology equipment,
which it had to import, he said.
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