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)?

Found something interesting?

Get better results by talking to an expert!
More essential person in AAPS!
Online Message