What is MAI CDMO Network?
MAI CDMO Network is a specialized B2B platform designed to transform the pharmaceutical outsourcing ecosystem. We connect pharmaceutical and biotech companies with a global network of pre-vetted Contract Development and Manufacturing Organizations (CDMOs) and Contract Manufacturing Organizations (CMOs).
Our mission is to simplify and expedite the complex process of finding, selecting, and contracting suitable manufacturing partners, leveraging advanced search filters and expert support to accelerate drug development and market entry for life-saving therapies.
Who is MAI CDMO Network for?
How can I contact a CMO or CDMO?
You can connect with a manufacturer in two primary ways:
Who can register?
Registration is open to two main groups:
Is registration free?
For CDMOs/CMOs, registration requires the selection of a collaboration plan upon sign-up. If no specific plan is chosen, it will be assumed that the user wishes to proceed with the Basic plan, which is free of charge. For commercial information regarding our premium plans and enhanced visibility features, please contact us at contact@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 contact@mai-cdmo.com and we´ll be happy to assist you with finding the right partner.
If I´m a CMO/CDMO and have a problem with my profile, how can I resolve it?
Email us at contact@mai-cdmo.com and we´ll resolve any issues or provide technical support as soon as possible.
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Adare Pharma is a global CDMO with sites in US and EU providing turnkey product development through commercial manufacturing expertise focused on oral dosage forms for the Pharmaceutical, Animal Health and OTC markets. Adare s proprietary technology platforms specialize in ODT s, taste masking and customized drug release.
Activity: FDF / DRUG PRODUCTS, SERVICES manufacturing
Uses: Human, Veterinary
Services: Regulatory services, Development services,...
Batch Size / Reactor: Small, Medium, Large
Compliance: ISO, EMA (EU GMP), FDA (cGMP), Health Canada...
Markets: DIGEMID (Peru), COFEPRIS (Mexico), INVIMA...
Accueil Sites Osny. Acquired in 2011, the Osny site specializes in the development and production of highly active solid pharmaceutical forms (hormonal and allergens). This 4,000 m2 pharmaceutical plant located 36 km northwest of Paris employs around a hundred people.
Activity: FDF / DRUG PRODUCTS manufacturing
Uses: Investigational, Commercial (Phase IV), Human
Services: Regulatory services, Development services,...
Batch Size / Reactor: Small, Medium
Compliance: EMA (EU GMP), FDA (cGMP), ANVISA (Brazil B-GMP),...
Markets: FDA (USA), EMA (EU), PMDA (Japan), MHRA (UK), NMPA...
Tubilux Pharma: registered office; manufacturing facility
Activity: FDF / DRUG PRODUCTS, SERVICES manufacturing
Uses: Commercial (Phase IV), Human, Veterinary
Services: N/A
Batch Size / Reactor: Medium, Large
Compliance: EMA (EU GMP), FDA (cGMP), TGA (Australia GMP),...
Markets: FDA (USA), EMA (EU), TGA (Australia), ANVISA...
Your cGMP-compliant CDMO for end-to-end services in the complex oral solids dosage forms field, based in Binzen Germany
Activity: FDF / DRUG PRODUCTS manufacturing
Uses: Investigational, Commercial (Phase IV), Human,...
Services: Development services, Manufacturing services,...
Batch Size / Reactor: Small, Medium, Large
Compliance: EMA (EU GMP), FDA (cGMP)
Markets: FDA (USA), EMA (EU)
Cell Therapy company with excess Cleanroom capacity
Activity: FDF / DRUG PRODUCTS, BIOLOGICS, SERVICES manufacturing
Uses: Investigational, Commercial (Phase IV), Human
Services: Regulatory services, Development services,...
Batch Size / Reactor: Small, Medium
Compliance: EMA (EU GMP)
Markets: EMA (EU)
Fully integrated CDMO solutions for Blow-Fill-Seal (BFS), sterile multidose, non-sterile multi-dose, sachets, capsules and tablets.
Activity: FDF / DRUG PRODUCTS, PARTICLE ENGINEERING manufacturing
Uses: Commercial (Phase IV), Human
Services: Regulatory services, Development services,...
Batch Size / Reactor: Small, Medium, Large
Compliance: ISO, EMA (EU GMP), FDA (cGMP)
Markets: FDA (USA), EMA (EU)
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
Compliance: ISO, EMA (EU GMP), FDA (cGMP), World Health...
Markets: FDA (USA), EMA (EU)
Seda Pharmaceutical Development Services specialises in integrated Pharmaceutical Development and Clinical Pharmacology.
Activity: FDF / DRUG PRODUCTS manufacturing
Uses: Investigational, Human
Services: Regulatory services, Development services,...
Batch Size / Reactor: Small, Medium
Compliance: ECOVADIS, MHRA (UK GMP)
Markets: DIGEMID (Peru), COFEPRIS (Mexico), INVIMA...
If you have any questions or suggestions, click here. We will be happy to assist you.
