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Engage the Right CDMO or CMO for Your Project

A decision-support platform designed for CMC, External Manufacturing, Procurement and Operations teams to accelerate partner selection with trusted data and guided insights.

Time Saving

From 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 Information

Manufacturer-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 Selection

Guided 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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Industry News

Check out the latest trends in the contract manufacturing industry

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Regulatory expertise can be the difference between a smooth veterinary drug approval and costly delays.

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WORLD CLASS CONTRACT MANUFACTURERS

Leading CMOs and CDMOs

United States North America
 
Adare Pharma | US
Adare Pharma | US

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...

France Europe
 
Cenexi SAS
Cenexi SAS

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...

Italy Europe
 
Content Group | Pomezia Plant
Content Group | Pomezia Plant

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...

Germany Europe
 
Glatt Pharmaceutical Services GmbH Co. & KG
Glatt Pharmaceutical Services GmbH Co. & KG

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)

Germany Europe
 
Green Phoenix Labs GmbH
Green Phoenix Labs GmbH

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)

Spain Europe
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PHARMALOOP S.L. - a Salvat Company
FDF / DRUG PRODUCTS PARTICLE ENGINEERING in Europe

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)

Switzerland Europe
 
Ophtapharm, a Sentiss Company
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

Compliance: ISO, EMA (EU GMP), FDA (cGMP), World Health...

Markets: FDA (USA), EMA (EU)

United Kingdom Europe
 
Seda Pharma Development Services
Seda Pharma Development Services

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...

Make Confident CMO / CDMO Decisions

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.


Accelerate Partner Identification

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.


High-Quality, Manufacturer-Provided Information

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.


Search CDMOs by Product Type

Users can identify CDMOs with proven experience in specific product categories, including:

  • Biologics: Cell and gene therapies, recombinant proteins, monoclonal antibodies and vaccines. [Search Biologics CDMOs]
  • Chemical-Synthetic: Small molecule APIs, intermediates and high-potency compounds. [Search Chemical CDMOs]
  • FDF / Drug Products: Solid orals, injectables, topicals and complex formulations. [Search FDF CDMOs]
  • Cosmetics: Contract manufacturing for skincare and personal care products.
  • Nutraceuticals / Food Supplements: Vitamins, functional foods and dietary supplements.
  • Services Only: Analytics, packaging, logistics or quality-focused CDMOs.

Filter by Intended Use

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.


Match by Stage of Development

MAI CDMO Network supports selection across the full product lifecycle:

  • Investigational stage: Preclinical development, clinical trial material and tech transfer (Phase I–III). [Search clinical CDMOs]
  • Commercial stage: Full-scale GMP manufacturing, validation and global supply (Phase IV and post-approval). [Search commercial CDMOs]

Lifecycle management and reformulation expertise can also be identified.


Choose the Right Batch Size

Production scale is a critical decision variable. Users can filter CDMOs by:

  • Small batches: Early-stage trials, personalized medicine and niche indications.
  • Medium batches: Regional launches and scale-up programs.
  • Large batches: Global commercial supply and long-term manufacturing.

Each CDMO profile specifies typical batch sizes and available scale-up pathways.


Target Specific Therapeutic Areas

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.


Consider Safety & Regulatory Complexity

Users can filter CDMOs based on containment, safety and regulatory requirements, including:

  • Occupational Exposure Bands (OEB 1–5) for potent and highly potent compounds
  • Biological Safety Levels (BSL 1–4) for biologics and advanced therapies
  • Narcotics, DEA (Schedules I–V) and other authorizations for controlled substances

This ensures alignment between product risk profile and manufacturing capabilities.


Certifications That Matter

Each CDMO is tagged with applicable certifications and market approvals, including:

  • GMPs from EMA, FDA, Health Canada, PMDA, NMPA, ANVISA and other authorities
  • International standards such as ISO, WHO GMP, NSF, BRCGS, ECOVADIS and Halal
  • Regional approvals across more than 20 global markets

This allows rapid verification of regulatory suitability for target markets.


Discover Full-Service Capabilities

MAI CDMO Network enables users to identify CDMOs offering end-to-end or specialized services, including:

  • Development services: Preformulation, tech transfer and scale-up
  • Manufacturing services: GMP production of drug substances and drug products
  • Analytical services: QC/QA testing, method development and validation
  • Packaging & logistics: Serialization, cold chain and international distribution
  • Regulatory support: Dossier preparation, CMC guidance and audits

Filters can be combined to identify full-service partners or highly specialized CDMOs.


A Practical Decision-Support Platform for Manufacturing Teams

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.


Start Exploring MAI CDMO Network

You can explore the manufacturing landscape or register to access extended information, guided selection features and direct engagement with relevant manufacturing partners.

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If you have any questions or suggestions, click here. We will be happy to assist you.

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Ascil
Liof Pharma
Cambrex
VIVUNT
Shilpa Biologicals
Histocell