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Formulation Research and Industrialization
The DiQi Pharma team is proficient in the development of prescription processes for solid and injectable formulations, and has rich experience in technology transformation and industrialization; Responsible for designing and implementing the prescription process for scaling up production batches for commissioned or cooperative clients, ensuring the smooth passage of pilot batches, validation batches, and dynamic verification batches simultaneously.
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Customized High-end Excipients
DiQi can customize PLGA with different end groups, molecular weights, intrinsic viscosity, and monomer ratios according to customers' personalized needs, with batch sizes up to kilogram level.
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DiQi Pharma can provide methodological research that meets NMPA, FDA, EMA, ICH, WHO, and other registration requirements. We have a professional team dedicated to researching various analytical methods throughout the entire lifecycle of drug development and supporting drug marketing and post marketing research.
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We can provide services such as early development and clinical pharmacology, BE trials, medical and scientific information, as well as clinical trial management and supervision.
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Global Application Affairs Pharmaceutical Support
Our registration affairs experts have over 30 years of experience in registration management, ensuring smooth and efficient completion of product registration. The company has a world-class quality system for drug formulation research and development. We establish a dedicated project team for each approved/signed project, equipped with formulation, analysis, registration, quality managers, and project managers to ensure project compliance and efficient completion.
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We have a 3Q confirmation plan for instruments and equipment that meets regulatory requirements, with the ability to optimize chromatographic systems and provide more efficient laboratory support.
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