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China is the world‘s second-largest pharmaceutical market, attracting numerous international pharmaceutical companies seeking marketing authorization for their active pharmaceutical ingredients and finished products. In this article from the latest issue of RF Quarterly, Lixue Zhang, MS, RAC, explores the quality considerations for international generic pharmaceutical products launched in the Chinese market. She also covers the fundamental principles of developing regulatory specifications, focusing on the stringent standards set by the Chinese Pharmacopoeia for residual solvents, heavy metals, and ignition residue. RAPS members get exclusive access to this article: https://bit.ly/4c1WkGv