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DMF registration and prior drug review systems to be eyed
Published: 2012-05-14 06:58:00
Updated: 2012-05-14 06:58:00
Drug manufacturers are obliged to register pharmaceutical raw materials in accordance with new DMF (drug master file) registration system. In addition, the government will implement a prior review system of new drugs before permission.
The Korea Food and Drug Administration announced yesterday a serious of measures to overhaul the current enforcement regulations of Pharmaceutical Affairs Law...
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