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Ruikangda Biomedical Technology - CDMO/CMO
We can provide the enzyme products and high-quality UDCA required for the conversion from CDCA to UDCA. We can also provide OEM services for high-quality or crude UDCA, according to the specifications specified by the customer
China
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Ensures stability across batches from gene editing to enzyme and UDCA production
GMP standards compliance to ensure the lowest levels of single, total, and C impurities within the product category
Customized services, supplying enzymes for UDCA conversion and crude UDCA products with purity from 85% to 99.99%
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Services
Drug Substance (CDMO/CRO)
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Contact Ruikangda (Shandong) Biomedical Technology for Contract Services Expertise
Connect with Ruikangda (Shandong) Biomedical Technology, a leading pharmaceutical company from China. They offer specialized Drug Substance (CDMO/CRO). Contact Ruikangda (Shandong) Biomedical Technology 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.