Efficient Partner DiscoveryUser-Friendly & Professional Search: Quickly find CDMOs tailored to your specific needs. Leverage our Intelligent Search Engine to find CMOs and CDMOs with proven expertise. Pre-Vetted Partners: Access a network of verified CDMOs for reliable collaboration. |
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Expert SupportConsulting Services: Get guidance on selecting the right contract manufacturer for your project. Do not hesitate to contact us or write to help@mai-cdmo.com. Transparent Quote Comparisons: Make informed decisions with easy access to multiple quotes. |
Accelerated Project DevelopmentReduced Time to Market: Streamline your selection process to focus on core activities. Improved Project Efficiency: Ensure smooth transitions from selection to execution. |
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2025-06-20
Explore MAI CDMO Services in Multiple Languages.
See more2025-04-30
Practical SEO strategies for CDMOs to increase online visibility and attract pharma and biotech partners.
See moreCompetence 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)
In today’s fast-moving pharmaceutical and biotech industries, selecting the right CDMO is critical to success. A reliable partner in contract manufacturing provides more than production support, it becomes a strategic asset that helps accelerate timelines, reduce risks, and ensure compliance.
At MAI CDMO, we’ve built a specialized platform designed to help you easily discover, compare, and connect with the right CDMO for your project. Whether you’re in early-stage development or looking to scale commercial manufacturing, our advanced search filters and expert guidance give you the clarity and confidence to move forward.
MAI CDMO lets you search based on the type of product you’re developing, ensuring the CDMO you select has proven expertise in your category:
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: Compliant contract manufacturing for skincare and personal care.
Nutraceuticals / Food Supplements: Vitamins, functional foods, and dietary supplements.
Services Only: Find CDMOs specializing in analytics, packaging, logistics, or QA.
Your product’s target market matters. That’s why we allow you to filter CDMO options by:
Human use: Prescription, OTC, and hospital-use pharmaceuticals. [Search by human use]
Veterinary use: Products for companion animals and livestock. [Search veterinary CDMOs]
Each CDMO is categorized so you can find partners with relevant expertise and licenses.
Depending on where your product is in the lifecycle, you’ll need a CDMO that can support either:
Investigational Stage: Preclinical, clinical trials, and tech transfer for Phase I–III. [Search clinical CDMOs]
Commercial Stage: Full-scale contract manufacturing with global distribution capability (Phase IV and post-approval). [Search commercial CDMOs]
You can also find CDMOs experienced in lifecycle management and reformulation.
Scale is key in Contract Manufacturing, and MAI CDMO lets you identify partners with the right production capacity:
Small Batches: Ideal for early-stage trials, personalized medicine, or niche markets.
Medium Batches: Flexibility for regional launches and scaling-up.
Large Batches: For global commercial supply and long-term contracts.
Each CDMO profile specifies their standard batch sizes and available scale-up paths.
With ATC-based filtering, you can search for CDMOs that focus on your therapeutic category, including:
Oncology, cardiovascular, CNS, respiratory, dermatology, infectious diseases, and more.
Specialized areas like radiopharmaceuticals, diagnostics, and nutrients.
Working with a CDMO that understands your therapeutic area can improve quality, reduce delays, and ease regulatory hurdles.
Our platform also allows you to filter CDMO options based on technical capabilities such as:
Occupational Exposure Bands (OEB 1–5): For low- to high-potency substances.
Biological Safety Levels (BSL 1–4): For biologics requiring containment.
DEA Licenses (Schedules I–V): For controlled substances under US regulation.
This ensures that your selected CDMO is equipped to safely handle your product.
Each CDMO listed on our platform is tagged with their certifications and market approvals. These include:
GMPs from EMA, FDA, Health Canada, PMDA, NMPA, ANVISA, and more.
International standards: ISO, WHO GMP, NSF, BRCGS, ECOVADIS, and Halal.
Regional authorities from over 20 global markets.
This helps you quickly verify which CDMOs are suitable for your regulatory targets.
Many of the CDMOs in our network offer comprehensive Contract Manufacturing and development services. You can search by:
Development Services: Preformulation, tech transfer, and scale-up.
Manufacturing Services: GMP production for drug substances and drug products.
Analytical Services: QC/QA testing, method validation, and release.
Packaging & Logistics: Serialization, cold chain, and international shipping.
Regulatory Support: Dossier preparation, CMC guidance, and audits.
You can combine filters to find full-service partners—or niche CDMOs for a single function.
Choosing the right CDMO is a complex process. MAI CDMO simplifies it by offering:
A searchable database of pre-vetted CDMO partners
Direct access to supplier profiles and commercial teams
Transparent quote comparison
Expert consultation and project support
Advanced filters across dozens of technical and regulatory dimensions
We reduce your time to decision, improve project efficiency, and give you access to the insights you need to choose the right contract manufacturing partner.
Whether you’re producing a niche biologic or launching a global brand, MAI CDMO helps you find the best CDMO for your needs. Sign up today and start your search with confidence—our experts are here to support you every step of the way.
If you have any questions or suggestions, click here. We will be happy to assist you.