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CN NMPA Seeks Opinions on Inclusion in 30-Day Channel for Innovative Drug Clinical Trial Review & Approval Applications
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China's National Medical Products Administration (NMPA) is publicly seeking opinions on the Announcement on Matters Related to the Optimization of Innovative Drug Clinical Trial Review and Approval (Draft for Comments).

The announcement proposes that applications for inclusion in the 30-day channel for innovative drug clinical trial review and approval should be for Category 1 innovative drugs (traditional Chinese medicine, chemical drugs, and biological products). Their application materials also have to be submitted as required and meet a range of conditions. For instance, the drugs should be key innovative drugs with national support.

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