>
API
CDMO
About us
Services
Contact supplier
Tianjin Pharmacn Medical Technology Co., ltd APIs on PharmaofferTianjin Pharmacn Medical Technology Co., ltd_1Tianjin Pharmacn Medical Technology Co., ltd_2Tianjin Pharmacn Medical Technology Co., ltd_3Tianjin Pharmacn Medical Technology Co., ltd_4
Show all images

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...

Address: 6 Haitaifazhan Sixth Road, Huayuan Industrial Area, Tianjin, China, 300000, Tianjin
China
China Local time:

Visit website

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:

Drug Substance

Production scale:

large
medium
Click here for more information on Eurofins audit reports
Currently Rephine has no report for this supplier. Contact them to let them know you're interested!

Response time:

Contact us
label.follow_us Follow us:
Employees:
300+
Established in:
2008

Services

Drug Substance (CDMO/CRO)

Intermediates
Pharmaceutical intermediates are compounds used in the production of APIs. CDMOs play a crucial role in synthesizing, scaling, and ensuring the quality of these intermediate compounds to support efficient drug manufacturing.
Contact supplier

Replies quickly

Small Molecule APIs
Small molecule APIs form the backbone of many pharmaceutical drugs due to their low molecular weight and ease of synthesis. They are widely used in treating a range of diseases and are typically produced through chemical synthesis in GMP-compliant facilities.
Contact supplier

Replies quickly

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.

Tianjin Pharmacn

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 development and testing of pharmaceutical products.

Preclinical Development: Our preclinical development services include in vitro and in Vivo studies to assess the safety, efficacy, and pharmacokinetic properties of drug candidates. We collaborate with reputable contract research organizations (CROs) andacademic institutions to conduct these studies in compliance with internationalregulatory guidelines.Clinical Trial Material Manufacturing: We have extensive capabilities in manufacturing clinical trial materials, ranging from small-scale batches for early-phase trials to large-scale production for late-phase trials. Our facilities adhere to strict quality standards and are compliant with international regulatory requirements.

Regulatory Support: We offer regulatory support services throughout the drug development process. Our regulatory affairs team assists clients in preparing andsubmitting regulatory dossiers, ensuring compliance with local and internationalregulations.Technology Transfer and Scale-Up: We assist in technology transfer from research laboratories to manufacturing sites, ensuring a seamless transition and maintaining process robustness. Our expertise in scale-up ensures efficient and cost-effective production of drug products.

Quality Control and Quality Assurance: We have a dedicated quality control and quality assurance team that ensures all our processes and products meet the highest quality standards. We follow strict quality control procedures and conduct rigorous quality checks at every stage of the drug development process.At Tianjin Pharmacn, we are committed to providing our clients with customized and high-quality drug development services. With our state-of-the-art facilities, experienced team, and regulatory expertise, we strive to support our clients in bringing safe and effective pharmaceutical products to market.