The road to R&D of new drugs in China - 1

Media interview

The US FDA recommends USP4 as the dissolution priority test method. Does the Chinese pharmaceutical industry see its value?

How to overcome the difficulties encountered in testing the dissolution of microspheres?  

What method will you recommend to test the microsphere dissolution?

What is your opinion on the policy of generic drug consistency evaluation?

How to effectively use the in vitro and in vivo correlation (IVIVC) for the dissolution testing of nanoparticle formulations (e.g., microspheres)?

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TPW 片剂样品前处理工作站可用于药物开发和质量保证中最常见药物测试的全自动样品前处理和分析,例如稳定性和均匀度测试等。

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