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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The goal is the reduce the cost for the health care system, because health cost a lot of money. So there are many possible initiatives, one is the “7 + 4 cities in China”, that’s one way to reduce the cost.
Samir HaddouchiManaging Director | SPS Parma Service