One-on-one communication with a professional business and technical team to clarify key needs such as product specifications, purity, application, capacity, cycle time, regulatory market conditions, etc., and provide the most suitable solution.
For custom synthesis, process optimization, and CMO/CDMO projects, rapid completion of route assessment, cost accounting, capacity matching, and risk prediction.
Providing standards/samples and basic information such as COA, HPLC, and MSDS to support customers in early-stage validation and selection.
Clarifying compliance requirements such as GMP, DMF, CEP, FDA, and EMA in advance to avoid later registration risks.
From raw material procurement, production, central control, testing, packaging to warehousing, full-process visible progress feedback ensures stable delivery times.
Leveraging the Jingmen production base, we strictly adhere to GMP management, ensuring delivery across all scenarios from mg-level pilot-scale to kg-level pilot-scale to ton-scale production.
Our R&D and production teams work in tandem to promptly resolve issues related to processes, quality, and stability, ensuring smooth project progress.
We provide a complete set of technical and quality documents simultaneously with each order, supporting customer R&D, filing, and on-site audits.
We support multiple batches, staggered batches, and urgent orders, adapting to the needs of customers at different stages of R&D, application, and commercialization.
• Establishing a complete batch traceability system for rapid response and efficient handling of quality issues.
• Providing stability data, sample retention support, and re-inspection services to ensure long-term product reliability.
• Providing continuous technical services such as process optimization, impurity research, and analytical method development and validation.
• Continuous iterative upgrades for long-term CRO/CDMO projects to improve yield and reduce costs.
• Provides complete drug registration documentation: COA, MSDS, process route, DMF/CEP support, and GMP compliance documents.
• Assists clients in completing domestic and international drug regulatory and client audits, providing full compliance support.
• Establishes safety stock and multi-source supply solutions to ensure uninterrupted supply for large orders and long-term partnerships.
• Provides value-added services such as annual framework agreements, price lock-in, and priority production scheduling.
Cosper adheres to a customer-centric, technology-driven, compliance-based, and delivery-guaranteed approach, building an integrated pharmaceutical service platform from R&D CRO → manufacturing CDMO → API supply → registration compliance → after-sales support. With its full-chain delivery capabilities, strong technical support, comprehensive after-sales system, and strict compliance management, Cosper has become a reliable and stable long-term partner for domestic and international pharmaceutical companies.
