The biosimilars market size in the Asia-Pacific was valued at 1.65 billion in 2023. The Asia-Pacific market is further predicted to grow at a CAGR of 31.60% from 2024 to 2029 and be worth USD 8.57 bn by 2029 from USD 2.17 bn in 2024.
Growing economies are seeing extensive development from the challenging medical therapeutic needs in the biosimilar industry. Increasing GDP and healthcare sector spending and demand for an economical therapeutic solution have contributed to this market's growth. Besides, biosimilars find their use in preventing and treating various chronic disorders like diabetes, cancers, cardiovascular diseases, etc. The demand for biosimilars is likely to rise in the coming years.While Asia-Pacific is the quickest-growing market for biosimilars due to low production costs, skilled and cheap labor availability, slender regulations laid down by governments, there are, however, high for manufacturing and sophistication, and the prevalence on the market of economically priced generic drugs, which has come forward as some of the biosimilars market's main constraints.
Countries like India, China, and South Korea are providing an enticing opportunity to develop and sell medicines in the region. Besides, these markets are generic-driven, creating a favorable incentive for the development and marketing of biosimilars. Also, the growing initiatives from the government and increasing investment in the healthcare sector in the region are providing lucrative growth opportunities for the region’s market to grow substantially. Large profit-churning blockbuster drugs are expected to lose their patent protection in APAC throughout the forecast period, and biosimilar firms are vigilant in filing marketing rights proposals.
The market for biosimilars in Asian nations is projected to develop significantly in the near future because of the readily available skilled labor, cheaper production costs, and fewer regulatory requirements. China, India, and Korea are all seeing active expansion in the biosimilars industry right now. Biosimilars provide rising Asian nations a significant opportunity to develop indigenous biologics and biotechnology capabilities. Domestic and regional biosimilar producers in Asian developing markets will be able to take the worldwide leader in the near future. Because the number of biosimilar producers in China is rapidly increasing, the Chinese FDA has established and approved biosimilars standards governing China's production, sale, and consumption. The primary drivers driving the market expansion in this area are the rising frequency of chronic diseases such as malignancies and increased investment in research and development efforts by key companies. Chronic diseases such as diabetes, cancer, and rheumatoid arthritis are becoming more common throughout the world, necessitating an ever-increasing demand for biologicals that are inexpensive and accessible in Asia Pacific countries (APAC).
In the research and marketing of biosimilars, China and India are also regarded to be prominent nations. While this type of product has been on the market for decades, the necessary rules and regulations have recently been adopted. The Chinese government has a variety of programs in place to help with biosimilar development and uptake. These include establishing transnational clinical centers, exchanging clinical data globally, expediting the special medication approval procedure, and improving clinical data security. The region's market growth is boosted by an expanding product pipeline and new product releases.
A few notable companies operating in the APAC Biosimilars market are Sandoz International GmbH, Wockhardt Ltd, Hospira, Inc., Teva Pharmaceutical Industries Ltd. Dr. Reddy’s Laboratories, Biocon Limited, Mylan, Inc., Zydus Cadila, Celltrion Inc., Roche Diagnostics, and Cipla Ltd.
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