Accelerated Partner Identification & Contact
Reliable Supplier-Provided Information
Search CDMOs by Product Type
Biologics
Cell and gene therapies, recombinant proteins, monoclonal antibodies and vaccines.
Search Biologics CDMOsSmall Molecules & APIs
Small molecule APIs and intermediates and high-potency compounds.
Search Chemical CDMOsCosmetics
Contract manufacturing for skincare and personal care products.
Nutraceuticals
Vitamins, functional foods and dietary supplements.
Support Services
Quality control & analysis, packaging or regulatory-focused service providers.
Filter by Intended Use
Match by Stage of Development
Investigational stage
Preclinical development, GMP clinical trial material and investigational new drugs (Phase I-III).
Search by clinical stageCommercial scale
Full-scale GMP manufacturing, tech-transfer, validation and global supply (Phase IV and post-approval).
Search by commercial scaleChoose the Right Batch Size
Small batches
Early-stage trials, personalized medicine and niche indications.
Search by small batchesTarget 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 Containment, Safety & Regulatory Complexity
Controlled Substances
Narcotics, DEA (Schedules I-V) and other authorizations.
A Platform Built on Compliance
Each provider is tagged with applicable certifications and compliance records, including: ⬢ GMPs from agencies such as EMA, FDA, Health Canada, PMDA, NMPA, ANVISA and other authorities. ⬢ International standards such as ISO, WHO GMP, NSF, BRCGS, EcoVadis and Halal certification. ⬢ Regulatory history and risk analysis are available to registered users. This enables rapid verification of regulatory suitability for target markets.
Discover Full-Service Capabilities
Development services
Process development and validation.
Manufacturing services
GMP and non-GMP production of drug substances and drug products, pilot plant availability, scale-up and tech transfer.
Analytical services
QC testing of raw materials and final products, and methods development and validation, filtering by sample type and assays.
Packaging & logistics
Primary and secondary packaging, serialization, labeling, storage and cold chain distribution.
Regulatory support
Dossier preparation, CMC guidance and applications support.
More Than a Directory
The public CDMO directory provides visibility into the collaborative platform and a limited demonstration of our proprietary matching technology. However, MAI CDMO Network offers a broader sourcing and partner evaluation infrastructure, including: ⬢ Expert support from the MAI CDMO Network team. ⬢ Detailed and structured database covering GMP-approved contract manufacturers worldwide and in-licensing opportunities, including business contact information to support efficient partner identification, evaluation, and outreach. ⬢ Guided sourcing and supply chain management tools, including workflow support, regulatory intelligence, risk analysis and project tracking features.