Suanfarma CDMO - CDMO/CMO

SUANFARMA CDMO provides integrated end-to-end solutions for development and commercialization of Intermediates and Drug Substances for Small Molecules. We are specialist in helping pharmaceutical, biotech and healthcare companies by providing leading innovative integrated services that compress timelines to market, maximizing succes.

We are a true One-Stop Shop partner through supply chain and value chain solutions.
On the supply...

Read full company description
Address: C. de Einstein, 8, 28108, Alcobendas, Madrid
Spain
Spain Local time:

Integrated innovative platforms for Technology Transfer (TT&GO®)

Fermentation, purification, and chemical synthesis technologies on the same site

Scalability from Laboratory and Pilot to Industrial scales

Our services:

CMO/CDMO

Production scale:

small
medium
large

Response time:

Service categories

Ingredient

API
Intermediates
label.follow_us Follow us:
Employees:
700+
Established in:
1993

Suanfarma CDMO in the media

Suanfarma unifies its industrial brands in a rebranding initiative under Suanfarma CDMO

Suanfarma unifies its industrial brands in a rebranding initiative under Suanfarma CDMO

Learn more

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.
Contact supplier

Replies quickly

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.
Contact supplier

Replies quickly

Contact Suanfarma CDMO for Contract Services Expertise

Connect with Suanfarma CDMO, a leading pharmaceutical company from Spain. They offer specialized CMO/CDMO - Contract (Development) Manufacturing Organizations, of which the services for CMO/CDMO include API, Intermediates. Contact Suanfarma CDMO 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.

Suanfarma CDMO


SUANFARMA CDMO provides integrated end-to-end solutions for development and commercialization of Intermediates and Drug Substances for Small Molecules. We are specialist in helping pharmaceutical, biotech and healthcare companies by providing leading innovative integrated services that compress timelines to market, maximizing succes.

We are a true One-Stop Shop partner through supply chain and value chain solutions.
On the supply chain, our unique capabilities allow to combine GMP industrial processes of fermentation, purification and chemical synthesis for a wide variety of small molecules (APIs and intermediates) and companies (Pharma, Biotech or Healthcare). Our technologies and expertise support us in achieving success, whether the molecule is innovative or generic.
On the value chain, SUANFARMA CDMO services run from preclinical supply up to commercial manufacturing, enabling it to continue supporting our clients as they take molecules through development and onto the market. At SUANFARMA CDMO we are guided by strict quality standards during all phases of production, from the selection of raw materials to manufacturing. Our facilities in Europe are in compliance with cGMP regulations requested by EMA and FDA standards.

We have worked on more than 37 different molecules, for more than 22 clients in Europe and other countries such as USA, Canada or Australia. Confidentiality, teamwork, flexibility and maximum communication are pillars of our work philosophy so that our client’s success becomes our success.

 

OUR CAPABILITIES

FERMENTATION AND PURIFICATION:

Small molecules fermentation and purification for human and veterinary use.
Different type of facilities from highly automated to flexible production plants.
Fermentation capacity with more than 2.000 m3.
Technologies applicable to purification including centrifugation, L-L and S-L separators, RVF, microfiltration, chromatography, filtration and dryers.
Pilot plant with optimized design to ensure the successful technology transfer and scaling-up phases.
Expertise managing different kind of organisms for fermentative production processes and for different type of molecules/applications.
Technical and GMP batches.

CHEMICAL SYNTHESIS:

Small molecules chemical synthesis for human and veterinary use.
Different type of facilities from highly automated to flexible production plants.
Reaction capacity with more than 800 m3.
cGMP Kilo-Lab for small scale processes.
Expertise in complex chemical reactions, carbonylation, hydrogenation, distillation, crystallization, cryogenic reactions, and for a wide variety of drug substances.
Stainless steel reactors, Hastelloy, special alloy and glass lined equipment, available for your projects.
Technical and GMP batches.