Registration Permit is Required for 28 Pharmaceutical Excipients
标签：drug manufacturing license, first batch of 28 pharmaceutical excipient, pharmaceutical excipient, SFDA • 2013年2月16日 • 0 条评论
The Regulation on Strengthening Supervison over Pharmaceutical Excipients has been effective since 1 Feb 2013. Since then, China starts to implement the management on pharmaceutical excipients based on their classification. For the new excipients and the excipients with high safety risk, the registration permit is required and excipient manufacturers need to get the Drug Manufacturing License. The other excipients are under control via the record-keeping approach.
