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EU GMP Instruction Strikes Chinese Medicine Sector
The No. 2011/62/EU regulation demands that the export products should meet the standards of GMP instruction, which at the same time brings new requirements and strikes towards Chinese
Medicine sector. The regulation will come into effect in July, 2013.
The new standard concentrates on the fake medicine which is much more referring to the non-registered raw material drug circulating in EU market, most of which comes from Chinese middle and small medicine factory.
The instruction further commands that all the medicine exporting to EU should present the written statement issued by the Supervisory and Managerial Department of the exporting country and be up to the requirements: First, the GMP instruction should meet the criterion of EU’s; Second, strict inspection on the manufactory corporation without advanced notice and taking measures once infringement are found; Third, reporting the cases offending EU GMP Instruction to EU.
Information source: International Business
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Published:2012-02-07
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