The DiQi Pharma formulation team is proficient in the development of prescription processes for solid and liquid formulations, and has rich experience in technology transformation and industrialization; Responsible for the design and implementation of the prescription process for scaling up production batches, ensuring the smooth passage of pilot batches, validation batches, and dynamic verification batches.

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.

We can provide early development and clinical pharmacology, BE trials, medical and scientific consulting, clinical trial management, supervision, and other services.

Our registration affairs experts have over 30 years of experience in registration management, ensuring smooth and efficient product registration. The company has a world-class quality management system for drug formulation research and development. We establish dedicated project teams for each approved/signed project, equipped with formulation analysis, registration, quality managers, and project managers to ensure compliance and efficient completion of the project.

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.