




Tianjin Pharmacn - CDMO/CMO
Tianjin Pharmacn Medical Technology Co., Ltd. is a leading CDMO (Contract Development and Manufacturing Organization) based in China. We provide comprehensive drug development services to pharmaceutical and biotechnology companies worldwide. Our company offers a wide range of services throughout the entire drug development lifecycle, including:
Formulation Development: We have a team of experienced scientists and formulation experts who work closely with our clients to develop optimized drug formulations. Our expertise covers various dosage forms, including tablets, capsules, injectables, and more.
Analytical Method Development and Validation: We provide robust analytical method development and validation services to ensure accurate and reliable analysis of drug compounds. Our state-of-the-art analytical facilities are equipped with advanced instruments to support the...

China

More than 150 patents based on independent intelligence

Expertise in anti-tumor, anti-diabetes and cardiovascular API and intermediates.

GMP facility with annual production capacity of 300M
Our services:
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Services
Drug Substance (CDMO/CRO)
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Contact Tianjin Pharmacn Medical Technology Co., ltd for Contract Services Expertise
Connect with Tianjin Pharmacn Medical Technology Co., ltd, a leading pharmaceutical company from China. They offer specialized Drug Substance (CDMO/CRO). Contact Tianjin Pharmacn Medical Technology 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.