Local Agency Support for Pharmaceutical Companies

With its registered company in China, BaiPharm serves as your reliable local authorized agent and provides support throughout the entire lifecycle of your drug product. From product development to regulatory approval, we ensure compliance with China local regulations and provide feasible regulatory guidance.

We act as a legally registered local entity in China, offering full lifecycle local agency support for global pharmaceutical enterprises — covering DMF filing, drug registration agency, regulatory liaison, post-approval variation, and professional DRP services.

Why Choose BaiPharm?

BaiPharm, a specialized subsidiary of REACH24H Consulting Group, is dedicated to pharmaceutical regulatory compliance. With offices in the U.S., EU, Japan, and South Korea, our expert team — including regulatory specialists, GxP auditors, consultants, certified toxicologists, and former inspectors — has supported over 600 pharmaceutical firms from 26 countries.

We act as a legally registered local entity in China, offering full lifecycle local agency support for global pharmaceutical enterprises. We cover DMF filing, drug registration agency, regulatory liaison, post-approval variation, annual report submission and adverse reaction reporting, alongside professional DRP services.

Boasting solid local regulatory experience and in-depth authority communication resources, we guide overseas clients through complex approval processes, ensure full compliance with Chinese regulations, and enable efficient, successful market entry.