Market revenue in 2023 | USD 385.2 million |
Market revenue in 2030 | USD 698.4 million |
Growth rate | 8.9% (CAGR from 2023 to 2030) |
Largest segment | Regulatory writing & publishing |
Fastest growing segment | Legal Representation |
Historical data | 2018 - 2022 |
Base year | 2023 |
Forecast period | 2024 - 2030 |
Quantitative units | Revenue in USD million |
Market segmentation | Regulatory Consulting, Legal Representation, Regulatory Writing & Publishing, Product Registration & Clinical Trial Applications, Other Services |
Key market players worldwide | Genpact Ltd, Icon PLC, Promedica International, Wuxi AppTec Co Ltd, Medpace Holdings Inc, Charles River Laboratories International Inc, Labcorp Drug Development, Cencora Inc, Pharmexon, QVigilance, Voisin Consulting Life Sciences, Accell, Criterium Inc., Freyr Solutions, PharmaLex, NDA Regulatory Service GmbH, BlueReg Group, Cambridge Regulatory Services |
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The databook is designed to serve as a comprehensive guide to navigating this sector. The databook focuses on market statistics denoted in the form of revenue and y-o-y growth and CAGR across the globe and regions. A detailed competitive and opportunity analyses related to biopharmaceutical regulatory affairs market will help companies and investors design strategic landscapes.
Regulatory writing & publishing was the largest segment with a revenue share of 31.49% in 2023. Horizon Databook has segmented the China biopharmaceutical regulatory affairs market based on regulatory consulting, legal representation, regulatory writing & publishing, product registration & clinical trial applications, other services covering the revenue growth of each sub-segment from 2018 to 2030.
China is one of the most attractive markets for the biopharmaceutical industry. The growing geriatric population and a large pool of middle-income group population are increasing the demand for innovative and cost-effective medicines, which is expected to attract major biopharmaceutical and medical device companies.
Seeking approval for new drugs is a primary challenge faced by biopharmaceutical companies, as a clinical trial application process requires 12 to 24 months. In contrast, approval process may require more than 6 years.
Along with national approvals, the new drug requires approval at the provincial and/or city level, which may require additional 4 to 5 years. Reforms in the healthcare sector in recent times are expected to streamline the approval process.
Horizon Databook provides a detailed overview of country-level data and insights on the China biopharmaceutical regulatory affairs market , including forecasts for subscribers. This country databook contains high-level insights into China biopharmaceutical regulatory affairs market from 2018 to 2030, including revenue numbers, major trends, and company profiles.
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