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Chem-stone (Guangzhou) - CDMO/CMO
Chem-Stone has a professional team of production, R&D, quality and sales. Our business model centers on CMO/CDMO services. We are ISO9001, ISO14001, and OHSAS18001 certified, ensuring professional CMO/CDMO services backed by a robust R&D team and comprehensive quality management...
China
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A high-tech enterprise with 13 own patents granted
Strong R&D system with ISO9001 / ISO14001 / OHSAS18001 certification
Provide professional CMO & CDMO service
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Service categories
Ingredient
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Chem-stone (Guangzhou) in the media
The 10th anniversary of the establishment of Chem-Stone
Learn moreListing of Chem-stone in Guangdong Equity Exchange Center
Learn moreWinning the third place in the Growth group of the 8th China Innovation and Entrepreneurship Competition
Learn moreOur services
Ingredient
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Contact Chem-Stone (Guangzhou) Co.,Ltd for Contract Services Expertise
Connect with Chem-Stone (Guangzhou) 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 Intermediates. Contact Chem-Stone (Guangzhou) 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.
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.