Date : 11 February 2026

| Pharmaceutical CRO and CDMO | Headquarters | Services |
| IQVIA | North Carolina, U.S. | Phase 1-4 clinical trials and advanced technologies |
| ICON plc | Dublin, Ireland | Full-service clinical development, biosimilar research, and adaptive trial designs |
| Parexel | Massachusetts, U.S. | Phase 1-4 clinical development, AI-driven trial simulation, and post-market surveillance |
| Charles River Laboratories | Massachusetts, U.S. | Preclinical discovery, laboratory models, efficacy testing ad safety assessment |
| Medpace | Ohio, U.S. | Integrated full-service clinic trials and central laboratory services |
| Lonza Group | Basel, Switzerland | Biologic manufacturing, API synthesis, and cell and gene therapy development. |
| Samsung Biologics | Incheon, South Korea | Large-scale biologics manufacturing, small molecule substances, drug product filling, and monoclonal antibodies production |
| Catalent | New Jersey, U.S. | Oral, respiratory drug delivery technologies, cell and gene therapy manufacturing |
| Boehringer Ingelheim | Ingelheim, Germany | Contract manufacturing for biologics, small molecule chemical innovation, and process development |
| Thermo Fisher Scientific | Massachusetts, U.S. | End-to-end solutions, API manufacturing, sterile fill-finish, and clinical trials logistics |
The global pharmaceutical CRO and CDMO market size was estimated at USD 254.65 billion in 2025 and is predicted to increase from USD 277.16 billion in 2026 to approximately USD 594.07 billion by 2035, expanding at a CAGR of 8.84% from 2026 to 2035.

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