The global biopharmaceutical CMO and CRO market was valued at USD 34.84 billion in 2024 and is projected to grow from USD 37.17 billion in 2025 to USD 62.36 billion by 2033, registering a CAGR of 6.68% during the forecast period (2025â2033). North America continues to dominate the market, holding the highest revenue share, largely driven by strong outsourcing demand, a robust biologics pipeline, and the presence of advanced service providers.
Biopharmaceutical Contract Manufacturing Organizations (CMOs) and Contract Research Organizations (CROs) play a vital role in the success of the pharmaceutical industry. CMOs provide end-to-end drug manufacturing services, while CROs support research, preclinical testing, clinical trials, and commercialization on a contract basis. The biopharmaceutical sector now accounts for over 20% of the global pharmaceutical industry, reflecting the rising demand for biologics and biosimilars.
The COVID-19 pandemic accelerated the outsourcing trend, as companies turned to CMOs and CROs to overcome supply chain challenges, meet rising vaccine demand, and maintain efficiency. As a result, North American CMOs and CROs benefitted significantly from this shift, positioning the region as the global leader.
Pharmaceutical and biotechnology companies are increasingly outsourcing development and manufacturing services. The growing pipeline of biologics and biosimilars is expected to drive demand, with smaller CMOs often growing faster than larger ones. For instance, the U.S. FDA approved 64 novel molecular entities and biologics in 2018, highlighting the scale of opportunities for outsourced services.
The industry is rapidly adopting advanced bioprocessing methods, single-use systems, and alternative business models to enhance capacity and reduce costs. This shift not only improves efficiency but also creates opportunities for CMOs and CROs to scale their operations and offer flexible solutions to biopharma clients.
North America accounted for nearly 35% of global revenue in 2021, making it the dominant region. The presence of SMEs lacking internal manufacturing capacity has strengthened collaboration with CMOs, while the U.S. market leads in biologics approvals and outsourcing partnerships.
Despite growth, the market faces challenges such as high initial investments, complex legal negotiations, and limited outsourcing by large, established biopharma companies. Intellectual property concerns, warranty agreements, and the high cost of biomanufacturing facilities are additional hurdles that slow expansion.
Strategic collaborations, R&D investments, and mergers & acquisitions are opening new growth avenues. A key example is the long-term partnership between Lonza and Moderna for commercial vaccine production, which reflects how CMOs are becoming critical to the industryâs future. With biopharma companies under pressure from rising costs and declining R&D productivity, outsourcing to CMOs and CROs is set to expand further.
These players are actively expanding through acquisitions, facility upgrades, and partnerships to strengthen their market presence.
The North America biopharmaceutical CMO and CRO market is well-positioned for sustained growth, thanks to its advanced biologics pipeline, outsourcing demand, and technological innovations. With a projected market value of USD 62.36 billion by 2033, the industry presents lucrative opportunities for both established and emerging players.
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