CDMO Services
Jiuzhou Pharma provides full-lifecycle contract development and manufacturing services to pharmaceutical companies worldwide. Our one-stop CDMO services span preclinical research, process R&D for APIs, DPs, peptides, and drug conjugates across all clinical phases and commercial production.
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Established Services
Jiuzhou Pharma provides global pharmaceutical companies with competitive API and intermediate process innovation, regulatory affairs support, and commercial production throughout the product life-cycle.
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Registration, Filing and Regulatory Support
Jiuzhou Pharma's regulatory affairs team has extensive experience in global drug registration and filing. We are committed to providing domestic and international customers with regulatory affairs solutions throughout the product lifecycle, including regulatory support, registration strategy planning and registration project management, bilingual application dossier preparation, registration inspection, deficiency letter responses, post-approval change management, and submission of applications.
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