Kraeber - CDMO/CMO

Kraeber + Co GmbH is an independent family owned business, established 1980 in Ellerbek on the outskirts of Hamburg, Germany. We sell Active Pharmaceutical Ingredients (APIs) and intermediates, which are synthetically derived products or biological substances of animal or plant origin. We supply our products worldwide to the pharmaceutical, cosmetic, biotechnology, nutraceutical industry and laboratories.

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Address: Waldhofstraße 14, 25474, Ellerbek
Germany
Germany Local time:

EU-GMP and DIN EN ISO 9001:2015

Pioneer in the fractionation of sheep plasma

Pure & sterile high-quality products

Our services:

CMO/CDMO

Production scale:

medium

Response time:

Service categories

Ingredient

API
Excipients

Biologics

Blood and blood products
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Employees:
30+
Established in:
1980

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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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Excipients
Excipients play a key role in drug formulation, enhancing stability, bioavailability, and patient acceptability. Their selection and quality control in production are vital for the overall effectiveness of pharmaceutical products, spanning tablets, capsules, and more.
Contact supplier

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Biologics

Blood and blood products
Blood and blood products are critical in transfusion medicine and therapies. Their processing involves rigorous screening and testing, ensuring safety and compatibility for use in surgeries, trauma care, and blood disorders, playing a life-saving role in healthcare.
Contact supplier

Replies quickly

Contact Kraeber & Co GmbH for Contract Services Expertise

Connect with Kraeber & Co GmbH, a leading pharmaceutical company from Germany. They offer specialized CMO/CDMO - Contract (Development) Manufacturing Organizations, of which the services for CMO/CDMO include API, Excipients, Blood and blood products. Contact Kraeber & Co GmbH 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.

Biologics

Biologics CMOs/CDMOs specialize in the manufacturing and development of biopharmaceutical products, which are typically derived from living organisms or biological sources such as proteins, antibodies, vaccines, and cell therapies. 


Biologics Contract Manufacturing Organizations (CMOs) and Contract Development and Manufacturing Organizations (CDMOs) encompass specialists in the production and development of biopharmaceuticals. These products, often derived from living organisms or biological sources, include proteins, antibodies, vaccines, and cell therapies. This sector includes biologics manufacturers, biopharma CDMOs, and companies dedicated to biologics development and biologic drug manufacturing.


Key Services Provided by Our Listed Biologics CMOs/CDMOs:


  • Advanced Biopharmaceutical Manufacturing: Utilization of cutting-edge biomanufacturing processes for the production of biologics, ensuring high purity, efficacy, and safety. This includes comprehensive biologics manufacturing and contract manufacturing biologics services.

  • Custom Antibody and Protein Development: Expertise in developing a range of biologic products, including monoclonal antibodies and therapeutic proteins, tailored to specific therapeutic needs. This is a key focus for many biologics companies and CDMO biotech firms.

  • Vaccine Production: Specialization in the manufacturing of vaccines using advanced technologies, contributing to global health and disease prevention efforts. This is a critical service offered by CMO biologics and biologics CDMO list members.

  • Cell Therapy Development: Capability to develop and manufacture innovative cell therapies, offering new treatment possibilities in regenerative medicine and oncology. This is a rapidly growing area within biologics development.

  • Regulatory Expertise: In-depth knowledge of the regulatory environment governing biologics, ensuring compliance with standards set by agencies like the FDA and EMA. This expertise is vital for all aspects of biopharmaceutical manufacturing.


Your Partner in Biologics Development and Manufacturing

Pharmaoffer provides a platform to connect with CMOs/CDMOs specializing in biologics. Our category ensures easy access to organizations that are equipped with the expertise and technology required for the complex development and manufacturing processes of biopharmaceutical products.

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.

Excipients

Excipients play a key role in drug formulation, enhancing stability, bioavailability, and patient acceptability. Their selection and quality control in production are vital for the overall effectiveness of pharmaceutical products, spanning tablets, capsules, and more.


Pharmaoffer connects you with Contract Development and Manufacturing Organizations (CDMOs) proficient in the supply and production of pharmaceutical excipients. These excipients are fundamental to drug formulation, significantly impacting stability, bioavailability, and patient acceptability of the final pharmaceutical product. This includes specialized services in Excipients Manufacturing and Excipient Production.


Key Services Provided by Our Listed CDMOs:


  • Diverse Range of Excipients: Supply of a wide variety of excipients suitable for various drug formulations, including tablets, capsules, and liquid medications. This is a critical aspect of Excipient Production.

  • Quality Control and Compliance: Rigorous quality control processes to ensure excipient purity and compliance with pharmaceutical standards. This is essential in Excipients Manufacturing.

  • Enhancement of Drug Properties: Expertise in selecting excipients that improve drug properties like solubility, stability, and patient acceptability.

  • Custom Excipient Solutions: Development of customized excipient solutions to meet unique formulation challenges and requirements.

  • Technical Support and Consultation: Providing technical expertise and consultation for optimal excipient selection and application in drug development.


Your Trusted Source for Excipient Solutions

Through Pharmaoffer, pharmaceutical professionals can find CDMOs that specialize in the critical component of drug manufacturing – excipients. Our platform ensures access to top suppliers offering high-quality, reliable excipient solutions for all types of pharmaceutical products.

Blood and blood products

Blood and blood products are critical in transfusion medicine and therapies. Their processing involves rigorous screening and testing, ensuring safety and compatibility for use in surgeries, trauma care, and blood disorders, playing a life-saving role in healthcare.


Pharmaoffer presents an array of Contract Development and Manufacturing Organizations (CDMOs) specializing in Blood and Blood Products. Our platform serves as a vital link for pharmaceutical professionals seeking specialized CDMOs in this critical area of healthcare.


Key Services Provided by Our Listed CDMOs:


  • Comprehensive Blood Processing: Advanced techniques for the collection, processing, and preservation of blood and blood components, ensuring the highest quality and safety.

  • Plasma Fractionation Expertise: Skilled in separating and purifying essential blood-derived products like immunoglobulins, clotting factors, and albumin.

  • Regulatory and Quality Compliance: Strict adherence to international standards and regulatory guidelines, including FDA and EMA, for blood product manufacturing.

  • Innovative Research and Development: Ongoing R&D to enhance blood product efficacy, safety, and shelf-life, meeting the evolving needs of the medical community.

  • Customized Blood Product Solutions: Tailored development and manufacturing services to meet specific clinical and therapeutic requirements.


Connecting You to Blood Product Experts

Through Pharmaoffer, you have access to CDMOs with specialized expertise in blood and blood product development and manufacturing. Whether it’s for transfusion medicine, therapeutic proteins, or novel blood-based products, our listed CDMOs are equipped to support your project's unique needs.

Kraeber


Kraeber + Co GmbH is an independent family owned business, established 1980 in Ellerbek on the outskirts of Hamburg, Germany. We sell Active Pharmaceutical Ingredients (APIs) and intermediates, which are synthetically derived products or biological substances of animal or plant origin. We supply our products worldwide to the pharmaceutical, cosmetic, biotechnology, nutraceutical industry and laboratories.