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...

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

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:

CMO/CDMO

Production scale:

large
medium

Response time:

Service categories

Ingredient

API
Intermediates
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Employees:
300+
Established in:
2008

Our services


Ingredient

API
APIs are the core of pharmaceutical products, determining the therapeutic efficacy. Their production involves complex synthesis, purification, and characterization processes, adhering to stringent regulatory standards. APIs are crucial in drug development for diverse medical conditions.
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Intermediates
Intermediates are crucial in the pharmaceutical supply chain, representing stages in the synthesis of APIs. Their production requires precision and control, impacting the quality and availability of final pharmaceutical products, across various therapeutic areas.
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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 CMO/CDMO - Contract (Development) Manufacturing Organizations, of which the services for CMO/CDMO include API, Intermediates. Contact Tianjin Pharmacn Medical Technology Co., ltd for free and discover if they are the perfect partner for your pharmaceutical needs.

CMO/CDMO - Contract (Development) Manufacturing Organizations

CDMOs and CMOs are pivotal in the pharmaceutical and biotech industries, offering specialized services in drug development and manufacturing. They assist in scaling up production from laboratory to commercial quantities, while adhering to strict regulatory standards. These organizations play a crucial role in the efficient and cost-effective production of medical and pharmaceutical products, ensuring quality and compliance at every stage.


Pharmaoffer's category for Contract Manufacturing Organizations (CMOs) and Contract Development and Manufacturing Organizations (CDMOs) encompasses a wide range of specialized services crucial to the pharmaceutical and biotech sectors. These organizations, often referred to as pharmaceutical CDMOs or drug CMOs, are instrumental in advancing drug development and manufacturing processes.


Key Functions of CMOs/CDMOs:


  • Drug Development and Manufacturing Expertise: Offering comprehensive services in drug development, from initial research and development to full-scale manufacturing. This includes CDMO services and CMO manufacturing, ensuring a seamless transition from concept to market.

  • Scalability Solutions: Assisting in scaling production from laboratory to commercial scale, meeting the demands of various projects while maintaining quality and efficiency. This is where the expertise of a full-service CDMO becomes invaluable.

  • Regulatory Compliance and Quality Assurance: Ensuring adherence to strict regulatory standards such as FDA and EMA guidelines, and implementing rigorous quality control measures throughout the manufacturing process. This includes operating within GMP certified facilities to guarantee the highest standards of production.

  • Cost-Effective Production: Providing efficient and cost-effective solutions for the production of medical and pharmaceutical products, enabling companies to focus on innovation and marketing. CMO contract manufacturing plays a key role in this aspect.

  • End-to-End Service Provision: From concept to commercialization, CMOs/CDMOs offer a range of services including process optimization, formulation development, clinical trial material production, and commercial manufacturing. This comprehensive approach is often referred to as Contract Development Manufacturing.


Connect with Leading CMOs/CDMOs

Through Pharmaoffer, you can explore and connect with a comprehensive range of CMOs/CDMOs. Our platform offers access to organizations that play a vital role in the efficient, quality-assured, and compliant production of pharmaceutical and medical products, supporting the industry's growth and innovation. Whether you're looking for a CDMO partner, CDMO solutions, or contract manufacturers in pharma, Pharmaoffer is your gateway to the best in the industry.

Ingredient

Ingredient CMOs/CDMOs specialize in the production of individual pharmaceutical ingredients, also known as active pharmaceutical ingredients (APIs) or drug substances. Their primary role is to synthesize, purify, and supply these chemical compounds in compliance with stringent quality standards.


Pharmaoffer's category for Ingredient Contract Manufacturing Organizations (CMOs) and Contract Development and Manufacturing Organizations (CDMOs) is dedicated to the production of individual pharmaceutical ingredients. These organizations, central to Pharmaceutical Ingredients Manufacturing, play a crucial role in synthesizing, purifying, and supplying active pharmaceutical ingredients (APIs) or drug substances, adhering to the highest standards of quality and compliance.


Key Services Provided by Ingredient CMOs/CDMOs:


  • API Synthesis and Production: Expertise in the synthesis of APIs, utilizing advanced chemical processes to produce high-purity pharmaceutical ingredients. This is a fundamental aspect of CDMO Ingredients services.

  • Stringent Quality and Purity Standards: Adherence to stringent quality and purity standards, ensuring that APIs meet all necessary pharmaceutical regulations and guidelines.

  • Supply Chain Reliability: Providing a reliable supply of essential pharmaceutical ingredients, crucial for the production of various medications.

  • Regulatory Compliance: Ensuring compliance with regulatory requirements, including FDA, EMA, and other global health authorities' standards.

  • Custom API Development: Offering tailored solutions for API development, addressing specific therapeutic needs and chemical properties.


Explore Specialized API Production Partners

Through Pharmaoffer, you can access a range of CMOs/CDMOs specializing in the production of pharmaceutical ingredients. Our platform connects you with providers who have the expertise and facilities necessary to produce APIs with the required purity, efficacy, and regulatory compliance.

API

APIs are the core of pharmaceutical products, determining the therapeutic efficacy. Their production involves complex synthesis, purification, and characterization processes, adhering to stringent regulatory standards. APIs are crucial in drug development for diverse medical conditions.


Pharmaoffer presents a comprehensive selection of Contract Development and Manufacturing Organizations (CDMOs) specializing in the production of Active Pharmaceutical Ingredients (APIs). Our platform caters to pharmaceutical professionals seeking expert services in API development and manufacturing, including API Manufacturing and API CDMO capabilities.


Key Services Provided by Our Listed CDMOs:


  • Complex Synthesis Capabilities: Expertise in intricate chemical synthesis processes, ensuring the production of high-quality APIs. This is a critical aspect of API production.

  • Rigorous Purification Processes: Advanced purification techniques to meet the highest purity standards essential for API efficacy and safety.

  • Detailed Characterization and Analysis: Thorough API characterization to ascertain structural integrity, stability, and compliance with pharmacopeial standards.

  • Compliance with Regulatory Requirements: Strict adherence to global regulatory guidelines, including FDA and EMA standards, ensuring the delivery of APIs that meet all necessary regulatory criteria.

  • Custom API Development: Tailored solutions for API development, catering to diverse therapeutic needs and specific drug formulations. This service is particularly important in the realm of Active Pharmaceutical Ingredients.


Your Ideal CDMO Partner for API Manufacturing

Pharmaoffer bridges the gap between pharmaceutical professionals and top CDMOs in the API sector. Whether it's for generic drugs or novel therapeutics, our listed CDMOs are equipped with the expertise and technology to support your API manufacturing needs, from small-scale lab production to large-scale commercial batches.

Intermediates

Intermediates are crucial in the pharmaceutical supply chain, representing stages in the synthesis of APIs. Their production requires precision and control, impacting the quality and availability of final pharmaceutical products, across various therapeutic areas.


Pharmaoffer's platform provides access to Contract Development and Manufacturing Organizations (CDMOs) proficient in producing pharmaceutical intermediates. These intermediates, essential components in the pharmaceutical supply chain, represent critical stages in the synthesis of Active Pharmaceutical Ingredients (APIs). This includes specialized services in Intermediates Manufacturing and Intermediates CDMO.


Key Services Provided by Our Listed CDMOs:


  • Precision in Intermediate Synthesis: Emphasis on precision and control in the synthesis processes, crucial for the quality of the final API. This is a key aspect of Intermediates Manufacturing.

  • Quality Assurance and Compliance: Stringent quality assurance protocols to ensure that intermediates meet all required standards and regulations. This is essential for any Intermediates CDMO.

  • Scalable Production Capacities: Ability to scale production of intermediates to match the demands of various pharmaceutical projects.

  • Wide Range of Intermediates: Production of a diverse array of intermediates, suitable for different therapeutic areas and drug formulations.

  • Collaborative Development Approach: Working closely with pharmaceutical companies to develop and produce intermediates that meet specific project requirements.


Connect with Intermediate Manufacturing Experts

Pharmaoffer connects you with CDMOs that have specialized expertise in the production of pharmaceutical intermediates. Our platform ensures you find the right partner capable of delivering high-quality intermediates, thereby impacting the efficacy and availability of final pharmaceutical products.

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.