Home / Engage the Right CDMO or CMO for Your Project
Time SavingFrom Months to Seconds: MAI CDMO Network enables pharma and biopharma teams to rapidly shortlist relevant CDMOs based on technical capabilities, regulatory compliance and therapeutic focus, among many other requirements. Direct Contact with Relevant Teams: Engage directly with the appropriate commercial or technical contacts, avoiding generic inboxes and accelerating meaningful discussions. |
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Reliable InformationManufacturer-Provided, Expert-Reviewed Data: CDMO and CMO profiles are created and maintained by the manufacturers THEMSELVES and reviewed by the MAI CDMO Network team to ensure accuracy, relevance and up-to-date technical information. |
Advanced & Guided CDMO SelectionGuided Search with Risk Insights: Registered users can access expert support and more detailed and unmasked information through a guided workflow that enriches search results with structured insights to help anticipate risks before engaging. |
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2026-02-12
Beyond Capacity: How Smarter Science is Redefining Biologics Manufacturing
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What truly matters when selecting a Contract Manufacturing Organization for clinical and commercial success
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2026-01-30
Regulatory expertise can be the difference between a smooth veterinary drug approval and costly delays.
See moreAdare 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...
Selecting a Contract Manufacturing Organization (CMO) or Contract Development and Manufacturing Organization (CDMO) is a strategic responsibility for pharmaceutical and biopharmaceutical teams. Professionals in CMC, External Manufacturing, Operations and Procurement must align technical feasibility, regulatory requirements, development stage, scale, timelines and long-term reliability, often under significant time pressure and across multiple stakeholders.
MAI CDMO Network is a decision-support platform designed to help teams identify, evaluate and connect with suitable CMOs and CDMOs through structured data, advanced filtering and direct access to relevant manufacturing organizations.
MAI CDMO Network enables users to rapidly shortlist relevant CDMOs based on technical capabilities, regulatory compliance, therapeutic focus, development stage and production scale, among many other requirements. What traditionally takes months can be reduced to a structured, traceable process.
Users can engage directly with the appropriate commercial or technical contacts, avoiding generic inboxes and ensuring that discussions start with the right technical and regulatory context.
Accurate and current information is essential for informed manufacturing decisions. On MAI CDMO Network, CMO and CDMO profiles are created and maintained by the manufacturers themselves, ensuring that capabilities, capacities and certifications reflect operational reality.
All profiles are reviewed by the MAI CDMO Network team to ensure clarity, relevance and consistency, providing a reliable foundation for partner evaluation.
Users can identify CDMOs with proven experience in specific product categories, including:
Products can be matched to CDMOs based on their intended market and licensing scope:
Each CDMO is categorized to reflect relevant authorizations and operational focus.
MAI CDMO Network supports selection across the full product lifecycle:
Lifecycle management and reformulation expertise can also be identified.
Production scale is a critical decision variable. Users can filter CDMOs by:
Each CDMO profile specifies typical batch sizes and available scale-up pathways.
Using ATC-based classification, MAI CDMO Network enables selection of CDMOs with experience in specific therapeutic areas, including oncology, cardiovascular, CNS, respiratory, dermatology, infectious diseases and more.
Specialized capabilities such as radiopharmaceuticals, diagnostics and nutrition-related products can also be identified.
Users can filter CDMOs based on containment, safety and regulatory requirements, including:
This ensures alignment between product risk profile and manufacturing capabilities.
Each CDMO is tagged with applicable certifications and market approvals, including:
This allows rapid verification of regulatory suitability for target markets.
MAI CDMO Network enables users to identify CDMOs offering end-to-end or specialized services, including:
Filters can be combined to identify full-service partners or highly specialized CDMOs.
MAI CDMO Network brings together structured manufacturer data, advanced filtering and guided selection workflows to support informed decision-making. The platform is designed to integrate naturally into the workflows of CMC, External Manufacturing and Procurement teams.
Whether evaluating new manufacturing options, building supply chain resilience or preparing future development milestones, MAI CDMO Network provides a clear and reliable starting point.
You can explore the manufacturing landscape or register to access extended information, guided selection features and direct engagement with relevant manufacturing partners.
If you have any questions or suggestions, click here. We will be happy to assist you.





