EU
officials clash with Chinese firm on drug factory inspection
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[September 13, 2018]
By Ben Hirschler
LONDON (Reuters) - European medicines regulators have issued a notice
that an ingredient for a generic brain cancer drug made in China does
not meet manufacturing standards, after inspectors were refused entry to
a factory run by Jiangsu Yew Pharmaceutical Co. Ltd.
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The incident, reported in a notice published this week on a database
maintained by the European Medicines Agency, is the latest example
of regulatory problems with bulk pharmaceutical substances
manufactured in China.
It follows a scandal over tainted supplies of the widely used heart
drug valsartan from Zhejiang Huahai Pharmaceutical, which led to
dozens of recalls around the world of finished tablets containing
the Chinese product.
U.S. officials have also recently recalled porcine thyroid active
ingredient from China due to inconsistent quality.
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In the latest case, Jiangsu Yew refused to allow a site inspection
by Hungarian officials, acting on behalf of Europe's drug regulatory
system. The rebuttal led the EU authorities to determine that its
supplies of temozolomide, used to treat brain tumors, did not comply
with good manufacturing standards.
The company's export director Henry Yang told Reuters via email that
the inspection was refused because Jiangsu Yew only made an
intermediate product, rather than an active pharmaceutical
ingredient (API), so an audit was not required.
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Manufacturers in China and India supply more than two-thirds of all
bulk pharmaceutical substances used in medicines, industry
executives estimate, with China accounting for the lion's share.
In recent years, U.S. and European regulators have increased
scrutiny of Asian drug factories following the adulteration of the
blood thinner heparin, which sickened hundreds and caused the deaths
of at least 81 Americans in 2007 and 2008.
(This version of the story has been refiled to add missing word
"notice" in second paragraph)
(Reporting by Ben Hirschler; Editing by Jan Harvey)
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