Compare US and Canadian CDMOs with FDA-registered facilities. Filter by manufacturing type, therapeutic focus, and certifications for domestic drug development and production.
482 companies listed
North America is the largest pharmaceutical market by revenue and home to hundreds of contract manufacturers. The US alone has over 500 FDA-registered drug manufacturing facilities. For US-based sponsors, domestic CDMOs reduce supply chain risk, simplify regulatory interactions, and shorten shipping timelines for temperature-sensitive biologics.
The BIOSECURE Act is reshaping outsourcing decisions. Companies that previously relied on certain Chinese CDMOs are actively reshoring manufacturing to North American and European partners. This has tightened capacity in biologics and cell therapy manufacturing, making early CDMO engagement more important than ever.
Where are the manufacturing clusters? The Boston-Cambridge corridor leads in biologics and cell therapy. The Research Triangle (NC) has strong small molecule and drug product capacity. San Francisco and San Diego anchor West Coast biologics. Canada offers competitive pricing through federal SR&ED tax credits, with hubs in Montreal and Toronto.
Every country below has its own page with a ranked CDMO list, a country-zoomed facilities map, and the local regulatory picture. Counts are live manufacturing-site totals.
United States
United States
Eastern GMP Consulting, LLC is an independent pharmaceutical and biotechnology consultancy based in North Wales, Pennsylvania, USA. The firm supports drug developers across CMC, technical operations, and quality functions, with a service focus on CDMO/CMO/CPO/CRO vendor selection and management, CMC project and program management, process development and technology transfer for both small and large molecules, and validation of equipment, processes, and packaging. Additional areas include clinical and commercial packaging, serialization, supply chain management, post-launch technical services, and regulatory and quality compliance support. This is led by a principal with three decades of industry experience in technical operations, CMC project leadership, and senior process validation roles at large pharmaceutical organisations.
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United States
eFortless Bio is a US-based company with no accessible website and minimal publicly available information. Search results return only unrelated companies (Fortis Life Sciences, Evotec). No evidence of drug manufacturing, CDMO, or CRO activities exists in available sources.