What is MAI CDMO?
MAI CDMO is a B2B platform designed to streamline the pharmaceutical supply chain. By connecting biopharmaceutical companies with the most suitable CDMOs and CMOs for their projects, we accelerate the development and commercialization of new drugs.
Who is MAI CDMO for?
How can I contact a CMO or CDMO?
Visit the page of the third-party manufacturer you`d like to contact. Fill out the form below the information and click the submit button.
Who can register?
Third-party developers and manufacturers of active pharmaceutical ingredients, drug substances, intermediates, drug products, cosmetics, nutraceuticals, medical devices, advanced therapies medicinal products and drug packaging can register.
Is registration free?
Registration is free. Afterward, if you are a contract manufacturer, you will receive an email with the different collaboration models available to enhance the visibility of your third-party manufacturing services. For commercial information, please email commercial@mai-cdmo.com.
How do I create a profile?
Go to the "Register" menu at the top, fill in the form, and submit it. Once the information is verified, you will get access to the profile.
If I`m looking for a CMO/CDMO and need help, where can I find it?
Email us at help@mai-cdmo.com and we`ll be happy to assist you.
If I`m a CMO/CDMO and have a problem with my profile, how can I resolve it?
Email us at support@mai-cdmo.com and we`ll resolve it as soon as possible.
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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...
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...
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...
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...
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...
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)
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...
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)
Discover answers to common questions in our FAQs at MAI CDMO. Learn how we connect pharmaceutical and biotech companies with leading CDMOs and CMOs to accelerate drug development and commercialization.
Find out who can register on our platform, from drug manufacturers to packaging and medical device companies, and how our registration process works.
Explore how our platform simplifies collaboration and enhances visibility for third-party manufacturers, helping you grow your business and bring new drugs to market efficiently.
If you have any questions or suggestions, click here. We will be happy to assist you.
