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Drug makers should submit vendor audit report in product license

Published: 2009-12-31 06:59:00
Updated: 2009-12-31 06:59:00
Those who intend to apply for a new product license should submit to the Korea Food and Drug Administration a vendor audit report within one month after such application from next year.

Under the vendor audit system, pharmaceutical manufacturers must audit their quality systems on a regular basis to ensure compliance with the appropriate regulations and standards.

An effective audit syste...

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