ZhenjiMed is China's only NMPA-authorized market access partner with an exclusive Pilot Zone facility — giving Western pharmaceutical companies a faster, compliant route to the world's largest patient population.
ZhenjiMed was founded to solve one of the hardest problems in global pharma: getting life-saving Western medications to Chinese patients efficiently, compliantly, and fast.
Operating from our exclusive authorization within the Qinhuangdao Pilot Zone, we sit at the intersection of regulatory expertise, clinical infrastructure, and deep NMPA relationships — a combination no other firm in China offers.
We are not consultants who advise from a distance. We are operators with a real facility, real staff, and real patient outcomes.
China's most unique regulatory environment for non-publicly listed medications
The Qinhuangdao Pilot Zone is China's designated area for non-publicly listed medications, allowing trials and treatments not available elsewhere in mainland China.
Our authorization comes directly from Chinese regulatory authorities, providing Western partners with the legal certainty they need to proceed with full confidence.
The Pilot Zone structure significantly reduces time from regulatory submission to patient treatment compared to standard NMPA channels, giving your drug a meaningful head start.
Our Qinhuangdao facility is not a consulting office — it is a full-scale medical center purpose-built for clinical treatment and trial facilitation. Western pharmaceutical partners can be confident that their medications reach patients in a controlled, professional, fully equipped environment.
We guide Western pharmaceutical companies through every stage of China's NMPA regulatory process — from initial assessment to approval strategy, documentation, and submission.
Through our Pilot Zone authorization, we manage patient recruitment, trial protocols, regulatory compliance, and real-time reporting for medication trials in China.
We handle NMPA import licensing, customs clearance coordination, cold-chain logistics partnerships, and all documentation for physical drug importation into China.
Our 4,000m² facility provides full clinical infrastructure for patient treatment — from intake and monitoring through to outcome reporting — all within our authorized Pilot Zone.
We evaluate your drug's regulatory profile, therapeutic area, and China market fit. You receive a clear feasibility report with a recommended pathway.
Our NMPA specialists design the optimal approval pathway — including Pilot Zone utilization where applicable — and agree timelines and milestones.
We prepare, translate, and submit all regulatory documentation, managing the NMPA dialogue on your behalf throughout the review process.
Our medical team prepares the clinical environment, recruits appropriate patients, and establishes monitoring protocols aligned with your trial design.
Patients receive treatment at our facility. You receive regular updates, regulatory reports, and outcome data — without the operational burden.
Full documentation available to verified pharmaceutical partners upon request.
Whether you're exploring the opportunity or ready to move forward, we'd like to understand your situation.
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