We support global healthcare companies in entering China, with a focus on pharmaceutical and medical device sectors.
We support China-based healthcare companies in expanding globally, with a focus on pharmaceutical and medical device sectors.
We support cross-border healthcare projects through end-to-end execution.
We do not stop at strategy — We deliver results
MediXin is a cross-border healthcare advisory and execution firm. We support global healthcare companies in entering China, and China-based companies in expanding internationally — from strategy to execution.
With deep expertise in China's healthcare policy, regulatory systems, and market access, MediXin translates complex environments into actionable pathways and ensures delivery through strong execution capability.
Our work focuses on enabling cross-border healthcare innovation, with particular strength in navigating China's regulatory landscape and supporting execution across Hong Kong, the Greater Bay Area, and global markets.

Kang Wei is the Founder and Strategic Lead of MediXin Group. She brings a unique combination of policy leadership, industry expertise, and execution capability.
Former Managing Director of RDPAC. Worked closely with multinational companies and regulatory authorities.
Founder of Greater Bay Area Alliance of Pharmaceutical Innovation (GBAAPI), connecting regulators, industry leaders, and global stakeholders.
Supports global healthcare companies entering China and China-based innovation expanding globally. We do not stop at strategy — we deliver results.
Vice President, Fresenius Kabi China | Senior Marketing Director & BU Head, Novartis Greater China

Annette Chiu is a highly experienced regulatory and medical affairs expert with over 30 years of experience across Hong Kong, China, and the Greater Bay Area. She has successfully led and accelerated the registration of more than 20 innovative products, including NCEs, biologics, and vaccines. She has extensive experience in regulatory strategy, pharmacovigilance, and GMP compliance, and has supported CFDI GMP inspections in China. Her therapeutic experience spans oncology, infectious diseases, vaccines, and chronic diseases. She also brings strong expertise in market entry strategy and engagement with regulatory authorities.
Identify the most viable pathway for market entry or expansion.
Define the optimal regulatory, clinical, and commercial approach.
Work with regulators, partners, and stakeholders to implement the strategy.
Ensure successful outcomes, from registration to commercialization.
Deep expertise in China's healthcare policy, regulatory and market access
Strong network across China, Hong Kong, the Greater Bay Area, and global markets
Proven end-to-end capability — from strategy to execution