Welcome to the Collaborative
Contract Manufacturing Platform
Find your partner
Find Your Perfect CMO / CDMO Partner with MAI CDMO Contract Manufacturing Platform
MAI CDMO: Your partner for pharmaceutical contract manufacturing outsourcing.
Discover the perfect CMO or CDMO for your project on our user-friendly platform. Connect with a global network of qualified Contract Manufacturing Organizations (CMOs) and Contract Development and Manufacturing Organizations (CDMOs) specializing in clinical trials and commercial manufacturing, synthetic and biological API production, finished forms manufacturing, packaging, and more. Save time, reduce costs, and ensure quality with our comprehensive network.
MAI CDMO simplifies the complex process of finding the right CMO/CDMO partner. Our platform allows you to easily search and connect with pre-vetted partners based on your specific needs. Filter by service, focus on expertise, and choose the location that best suits your project.
Discover how MAI CDMO can accelerate your drug development and bring your life-saving treatments to market faster. We offer valuable resources to empower you throughout the pharmaceutical outsourcing process, including efficient partner discovery and expert support.
Contact us today to learn more about how MAI CDMO's platform can streamline your pharmaceutical outsourcing journey. Let us help you bring your life-saving treatments to market faster and reach patients worldwide by joining the online collaboration ecosystem.
WORLD CLASS CONTRACT MANUFACTURERS
Leading CMOs and CDMOs
Italy
Europe
Aenova Group - Location Latina, Italy
Competence Center animal health products and sterile technologies.
Activity: FDF / DRUG PRODUCTS, BIOLOGICS manufacturing
Uses: Investigational, Commercial (Phase IV), Human,...
Services: Regulatory services, Development services,...
Batch Size / Reactor: Small, Medium, Large
Certifications: EMA (EU GMP), FDA (cGMP), ANVISA (Brazil B-GMP),...
Markets: FDA (USA), EMA (EU), ANVISA (Brazil), Russian...
United States
North America
Cambrex Charles City
Our 400+ team members in Charles City specialize in late-phase and commercial API development and cGMP manufacturing.
Activity: CHEMICAL-SYNTHETIC manufacturing
Uses: Investigational, Commercial (Phase IV), Human
Services: Development services, Manufacturing services,...
Batch Size / Reactor: Small, Medium, Large
Certifications: EMA (EU GMP), FDA (cGMP), Health Canada (Canada...
Markets: FDA (USA), EMA (EU), PMDA (Japan), Health Canada...
France
Europe
Cenexi Hérouville Saint Clair
The Hérouville-Saint-Clair site, located near Caen, in Normandy, specializes in the manufacture and filling of injectable and non-injectable sterile liquid products. It has a pharmaceutical surface area of 17,900 m2 over 10 hectares and employs 290 people.
Activity: FDF / DRUG PRODUCTS manufacturing
Uses: Investigational, Commercial (Phase IV), Human
Services: Regulatory services, Manufacturing services,...
Batch Size / Reactor: Small, Medium
Certifications: EMA (EU GMP), FDA (cGMP), NMPA (China GMP), ANVISA...
Markets: FDA (USA), EMA (EU), PMDA (Japan), MHRA (UK), TGA...
Spain
Europe
Grifols International | Barcelona Plant
Sterile manufacturing solutions (small molecules) in flexible bags and vials.
Activity: FDF / DRUG PRODUCTS manufacturing
Uses: Investigational, Commercial (Phase IV), Human,...
Services: Regulatory services, Development services,...
Batch Size / Reactor: Small, Medium, Large
Certifications: ISO, EMA (EU GMP), FDA (cGMP), Health Canada...
Markets: FDA (USA), EMA (EU), PMDA (Japan), Health Canada...
United States
North America
Lannett CDMO
Lannetts main manufacturing site sits in Seymour, Indiana, and includes capabilities for Oral Solid Dose (OSD) and Liquids.
Activity: FDF / DRUG PRODUCTS manufacturing
Uses: Investigational, Commercial (Phase IV), Human,...
Services: Regulatory services, Development services,...
Batch Size / Reactor: Small, Medium, Large
Certifications: EMA (EU GMP), FDA (cGMP), Health Canada (Canada...
Markets: COFEPRIS (Mexico), FDA (USA), EMA (EU), PMDA...
Switzerland
Europe
Ophtapharm, a Sentiss Company
Ophtalmic and Otic - Solutions, suspensions, emulsions, ointments and gels - FDA Approved facility
Activity: FDF / DRUG PRODUCTS manufacturing
Uses: Investigational, Commercial (Phase IV), Human,...
Services: Regulatory services, Development services,...
Batch Size / Reactor: Small, Medium, Large
Certifications: ISO, EMA (EU GMP), FDA (cGMP), World Health...
Markets: FDA (USA), EMA (EU)
United States
North America
Pharmaron Coventry Site (US)
Small Molecule (RSM/APIs) Commercial Facility
Activity: CHEMICAL-SYNTHETIC manufacturing
Uses: Investigational, Commercial (Phase IV), Human,...
Services: Development services, Manufacturing services
Batch Size / Reactor: Small, Medium, Large
Certifications: ISO, FDA (cGMP), ECOVADIS
Markets: FDA (USA), EMA (EU), PMDA (Japan), Health Canada...
Spain
Europe
VIVUNT PHARMA
CDMO Sterile Oncology Drugs
Activity: FDF / DRUG PRODUCTS manufacturing
Uses: Investigational, Commercial (Phase IV), Human
Services: Manufacturing services, Analytical / QC services,...
Batch Size / Reactor: Small, Medium, Large
Certifications: EMA (EU GMP)
Markets: EMA (EU)
Get in touch
Contact directly the technical and commercial teams of the ideal CMO or CDMO for your project.
PHARMALOOP S.L. - a Salvat Company
ChemCon GmbH
HISTOCELL S.L.
Industry News
Check out the latest trends in the contract manufacturing industry
MAI CDMO Launches Website in 5 Languages to Support Global Clients
2025-06-20
MAI CDMO’s website is now available in English, Spanish, German, Italian, and French. Discover our CDMO services with a smoother, multilingual experience.
See more
SEO for CDMOs: How to Think Like Your Searcher
2025-04-30
Practical SEO strategies for CDMOs to increase online visibility and attract pharma and biotech partners.
See moreMAI CDMO is your one-stop shop for streamlining the pharmaceutical outsourcing process. Our B2B platform connects you with a global network of qualified Contract Manufacturing Organizations (CMOs) and Contract Development and Manufacturing Organizations (CDMOs), saving you time and resources.
Reduce Development Time and Costs:
Finding the right CMO/CDMO partner can be a complex and time-consuming process. MAI CDMO simplifies this by providing a user-friendly platform to search and connect with pre-vetted partners based on your specific needs. Our comprehensive directory allows you to:
- Filter by Service: Narrow down your search based on required services like clinical trial manufacturing, API production, or packaging and labeling.
- Focus on Expertise: Find CMOs specializing in your therapeutic area, ensuring they have the experience to handle your project effectively.
- Location Matters: Connect with CMOs in your preferred region or explore global options for cost optimization.
Streamline Clinical Trials:
With MAI CDMO, you can easily find qualified partners for streamlining your clinical trial manufacturing process. Our platform helps you:
- Reduce Delays: Quickly connect with CMOs with proven experience in clinical trial manufacturing, ensuring timely project completion.
- Ensure Quality: Find partners meeting the highest quality standards to maintain regulatory compliance throughout your clinical trials.
- Optimize Costs: Compare quotes from various CMOs to negotiate the most cost-effective solution for your clinical trial needs.
More Than Just a CDMO Directory:
MAI CDMO goes beyond simply connecting you with CMOs and CDMOs. We offer valuable resources to empower you throughout the pharmaceutical manufacturing outsourcing process, including:
- Industry Insights: Access helpful articles and guides on navigating the complexities of pharmaceutical manufacturing outsourcing.
- Best Practices: Learn from industry experts on best practices for selecting and working with CMO partners.
- Success Stories: Discover how other pharmaceutical companies have leveraged MAI CDMO to achieve their drug development goals.
Bring Your Treatments to Market Faster:
Contact us today to learn more about how MAI CDMO´s platform can simplify your pharmaceutical outsourcing journey and accelerate your drug development timeline. Let us help you bring your life-saving treatments to market faster and reach patients worldwide.
Contact us
If you have any questions or suggestions, click here. We will be happy to assist you.
