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REPORT
[Updated] China Pharma Guidelines: Nonclinical Study, Clinical Trial, Marketing Authorization and More
Oct 17, 2023
Q&A
China CDE Q&A | BE Study, Reference Listed Drug, and Quality & Therapeutic Equivalence Evaluation
Aug 30, 2022
INTERPRETATION
How to Submit Abbreviated New Drug Application (ANDA) for Generic Drugs in China
May 18, 2022