Biosimilars Market Regional Analysis

Skyquest Technology's expert advisors have carried out comprehensive global market analysis on the biosimilars market, covering regional industry trends and market insights. Our team of analysts have conducted in-depth primary and secondary research to provide regional industry analysis and forecast of biosimilars market across North America, South America, Europe, Asia, the Middle East, and Africa.

Biosimilars Market Regional Insights

North America dominates the global market at present, with the United States experiencing rising uptake after a record number of FDA approvals in 2023, including biosimilars for Humira (adalimumab), one of the world's top-selling medicines. Europe continues to lead with more than 60% of global sales of biosimilars because of well-established regimes and early uptake by prescribing physicians.

Asia-Pacific, particularly China, India, and South Korea, on the other hand, is expected to witness significant growth following strong government push, local capability to manufacture, and increasing needs for affordable biologics.

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Global Biosimilars Market size was valued at USD 24.3 billion in 2023 and is poised to grow from USD 28.38 billion in 2024 to USD 98.31 billion by 2032, growing at a CAGR of 16.8% during the forecast period (2025-2032).

Some of the notable contributors include Pfizer, Novartis (Sandoz), Amgen, Biocon Biologics, Samsung Bioepis, and Celltrion. These players use cutting-edge manufacturing, biosimilar interchangeability strategies, and competitive pricing to battle in the market. Some of the upcoming players such as Alvotech, Coherus BioSciences, and Polpharma Biologics are also emerging, making a difference through innovation and affordability. As biosimilar adoption increases, competition intensifies, fostering market growth and affordability of biologic treatments globally.

The growing prevalence of chronic diseases like cancer, diabetes, and autoimmune diseases is propelling the need for cheap biologic treatments. Biosimilars ensure cheaper substitutes to pricey biologics, enhancing patients' access to life-sustaining medicines. This surging demand for long-term therapeutic solutions continues to boost uptake for biosimilar drugs.

Regulatory bodies such as the FDA and EMA are simplifying biosimilar approval procedures, resulting in more market entries. Faster approvals encourage competition, driving down costs and expanding accessibility. Healthcare providers and payers are more inclined to adopt biosimilars, causing a surge in market penetration and reshaping pricing strategies for both originator biologics and biosimilars.

North America continues to lead the global biosimilars market share, driven by a robust regulatory framework, significant R&D investments, and a surge in biosimilar approvals.

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Biosimilars Market

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