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Plants in:
Established in: 2014
Production scale:
small
medium
large
Employees: 1000+
22 years of production experience
6 workshops and 9 production lines which has 100t/month production capacity
4 USDMFS & 5 CEPS & 200+ Patents
All certificates
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CDMO-CMO
Plants in:
Established in: 1934
Production scale:
large
small
medium
Employees: 1500
Full-Service CDMO with End-to-End Solutions
Reliable Global Distribution Operating in over 70 countries
Specialized in hormones, crystal-suspensions and complex injectables
All certificates
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CDMO-CMO
Plants in:
Established in: 1886
Production scale:
medium
small
Employees: 275+
Raw materials, CMO and OTC products
Two GMP certified locations
Customisable (small-sized) packages
All certificates
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CDMO-CMO
Plants in:
Established in: 2023
Production scale:
small
medium
large
Employees: 1000+
Expertise in Conventional, Complex, and Niche Chemistries
End-to-end Support from early development to Commercial Phases
Comprehensive Analytical Support Facilities
All certificates
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CDMO-CMO
Plants in:
Established in: 2006
Production scale:
small
medium
Employees: 20
Quality Assurance: Products are manufactured from the finest raw materials and undergo rigorous testing.
Tailored Customisation & Compliance: Providing end-to-end solutions to meet your business
Dependable Expertise and Supply: Backed by years of industry experience and a robust supply chain.
All certificates
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CDMO-CMO
Plants in:
Established in: 1964
Production scale:
small
medium
large
Employees: 135+
Market leader in Switzerland
Small and medium batch sizes
Pharmaceutical raw materials with a herbal or synthetic basis
All certificates
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CDMO-CMO
Plants in:
Established in: 2019
Production scale:
large
Employees: 10+
Focused on pharmaceutical industry
Reasonable price for the customers
Full service from R&D stage to commercial stage
All certificates
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CDMO-CMO
Plants in:
Established in: 1965
Production scale:
small
medium
large
Employees: 600+
Pharmaceutical-quality dextrans meeting the highest standards and complying with major pharmacopeias
Manufactured in a cGMP facility in Denmark, inspected by both the FDA and EMA
Documented quality and certifications from the US FDA and EDQM for smooth regulatory submission
All certificates
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CDMO-CMO
Plants in:
Established in: 1952
Production scale:
small
medium
large
Employees: 550+
API manufacturing (Innovators, Generics and Highly Potent)
A tailor-made and flexible service approach
State-of-the-art analytical services including solid form and QbD laboratories
All certificates
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CDMO-CMO
Plants in:
Established in: 2013
Production scale:
medium
Employees: 25+
ISO9001 certified
Drug R&D center (in Hangzhou)
From lab scale (mg/g) to commercial scale (kgs/tons)
All certificates
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CDMO-CMO
Plants in:
Established in: 2021
Production scale:
small
Employees: 19
API, Intermediates, Building Blocks, Impurities, Amino acids and Peptides
Small quantity APIs to commercial scale
GMP and USFDA certification based on quantity, order, assignment.
All certificates
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CDMO-CMO
Plants in:
Established in: 1980
Production scale:
medium
Employees: 30+
EU-GMP and DIN EN ISO 9001:2015
Pioneer in the fractionation of sheep plasma
Pure & sterile high-quality products
All certificates
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CDMO-CMO
Plants in:
Established in: 1997
Production scale:
small
medium
Employees: 140
Top-tier adherence to global pharmaceutical standards including GMP, FDA and EMA
Specialized advanced chemistry laboratory focused on upscaling and GMP transfer processes
Comprehensive analytical services to meet precise client specifications.
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CDMO-CMO
Focus on innovative nutritional and dietary supplements.
Comprehensive services from formulation to manufacturing and packaging.
Strong commitment to quality and customer satisfaction in the wellness sector.
All certificates
Replies slower than most
CDMO-CMO
Plants in:
Established in: 1987
Production scale:
medium
small
large
Employees: 50+
ISO 9001:2015 & SGS audited supplier
One-stop CDMO Solutions for APl and Key intermediates
Specialized in APIs & Pharmaceutical Intermediates for 37 years
All certificates
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CDMO-CMO
Plants in:
Established in: 1989
Production scale:
large
Employees: 5000+
6 production facilities approved by USFDA, AGES-Austria, PMDA, WHO
R&D Centers with capabilities of ANDAs, DMFs and NDDS
462+ patents filed for drug substances and polymorphs
All certificates
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Plants in:
Established in: 1982
Production scale:
small
Employees: 30+
Modern GMP facility
Team of academics and technical experts
Small to large batch sizes possible
All certificates
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CDMO-CMO
Customized supplement manufacturing with a focus on quality and compliance.
Wide range of capabilities from capsules to powders and liquids.
Strong emphasis on turnkey solutions and timely delivery.
All certificates
Replies slower than most
Plants in:
Established in: 2008
Production scale:
large
medium
Employees: 300+
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
All certificates
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CDMO-CMO
Plants in:
Established in: 1972
Production scale:
medium
Employees: 1,000+
EU-GMP for APIs and CEP for certain APIs
Exporting to over 50 countries worldwide
Long-standing technological advantage in adamantane, quinuclidine and nitrofurane chemistry
All certificates
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CDMO-CMO
Plants in:
Established in: 1951
Production scale:
medium
Employees: 455+
Largest Polish manufacturer of pharmaceuticals and a leader of the Polish pharmaceutical market.
FDA approved european manufcaturing facilities
Export APIs to more than 60 countries worldwide
All certificates
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CDMO-CMO
Specialized in custom nutraceuticals and dietary supplements manufacturing.
Innovative approach to product formulation and packaging.
Strong emphasis on natural and clean label products.
All certificates
Replies slower than most
CDMO-CMO
Plants in:
Established in: 2012
Production scale:
medium
Employees: 180
A high-tech enterprise with 13 own patents granted
Strong R&D system with ISO9001 / ISO14001 / OHSAS18001 certification
Provide professional CMO & CDMO service
All certificates
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CDMO-CMO
Plants in:
Established in: 1993
Production scale:
small
medium
large
Employees: 600
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
All certificates
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Looking for CMO/CDMO Services?
Find a list of providers specializing in CMOs/CDMOs Services for Ingredient. Navigate through our extensive selection to identify the supplier that aligns with your specific needs.
Pharmaoffer makes it easy and convenient to send inquiries at no cost. Directly connect with your chosen supplier and take the first step towards fulfilling your pharmaceutical needs easily and efficiently.
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.
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.
