The NMPA are not some backwater bureaucracy. It's a developed mass pharmaceutical market that includes most of the top 20 BP selling their drugs into the domestic market. Moreover, none of the Chinese pharmaceutical companies are going to start clinical trials on a counterfeit PPS formula before the real deal is a proven under their clinical rules. Even then they would be excluded from doing so for an extended period. Many relevant examples here so more informed posting is required. Not directed at you Dungiven
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