The measures for the supervision and administration of drug production will be officially implemented on July 1, 2020, and the National medical product administration published the implementation plan on April 3. Since July 1, 2020, the new measures shall be implemented for the production license of preparations, APIs and Chinese herbal pieces., the drug production license applications before July 1, which have been accepted but not approved shall be handled in accordance with the new management measures after July 1.The existing “drug production license” shall continue to be valid within the validity period. Change, reissue and reissue after July 1,Read More →
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