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Chongqing Sintaho - CDMO/CMO
Specialize in cGMP and Massive Production Capacity Capability: Our company is dedicated to providing comprehensive CDMO services spanning the lab scale to commercial supply. In the lab scale phase, we focus on process development, analytical method development, and molecular characterization to lay a solid foundation for R&D. Moving into the pilot scale phase, we conduct rigorous analytical method validation, process optimization, and perform small-scale production, During the clinical trial sample manufacturing phase, we offer customized samples for PhaseⅠto Ⅲ clinical trials, with options for GMP or non-GMP manufacturing. In the GMP large-scale production phase, we ensure cost-effectiveness, supply chain timeliness, and full support for regulatory submissions. In the commercial supply phase, we maintain the stability of the supply chain. Our company also excels in confidentiality...
China
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Certified by US FDA
Well-Established Environmental, Health & Safety Protocols
Seasoned Project Execution Team
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Drug Substance (CDMO/CRO)
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Contact Chongqing Sintaho Pharmaceutical Co., Ltd. for Contract Services Expertise
Connect with Chongqing Sintaho Pharmaceutical Co., Ltd., a leading pharmaceutical company from China. They offer specialized Drug Substance (CDMO/CRO). Contact Chongqing Sintaho Pharmaceutical Co., Ltd. for free and discover if they are the perfect partner for your pharmaceutical needs.
Drug Substance (CDMO/CRO)
Drug Substance CDMOs and CROs provide essential services in the development and manufacturing of active pharmaceutical ingredients (APIs). These organizations specialize in early-stage research, process development, and GMP-compliant manufacturing of drug substances for clinical and commercial use.
Pharmaoffer's Drug Substance CDMO/CRO category includes partners with expertise in small molecules, biologics, peptides, and complex chemistry, all operating under strict regulatory compliance. These providers help companies scale from lab to market efficiently and cost-effectively.
Key Functions of Drug Substance CDMOs/CROs:
API Research and Development: Providing early-stage discovery support, custom synthesis, and process optimization to streamline the development of drug substances.
Process Scale-Up and Tech Transfer: Transitioning from bench-scale to pilot and commercial scale production with validated methods and reproducibility.
GMP Manufacturing: Delivering high-quality API batches in GMP-certified environments, adhering to FDA, EMA, and other international standards.
Analytical Services: Offering comprehensive analytical method development and validation to ensure consistent quality and regulatory compliance.
Flexible and Specialized Capabilities: From small molecule synthesis to biologic and peptide manufacturing, these partners provide specialized services tailored to product-specific needs.
Explore Leading API CDMOs and CROs
Pharmaoffer connects you with trusted CDMOs and CROs for drug substance development. Our platform enables seamless access to specialized service providers equipped to support your API lifecycle from discovery to commercialization.