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市場調查報告書
商品編碼
1749704
醫學寫作AI的全球市場:類別·各部署方式·各最終用途·各地區的評估,機會及預測 (2018~2032年)Global AI in Medical Writing Market Assessment, By Type, By Deployment Mode, By End-use, By Region, Opportunities and Forecast, 2018-2032F |
全球醫學寫作人工智慧市場預計將從 2024 年的 8.4542 億美元增長到 2032 年的 20.3505 億美元,在 2025-2032 年預測期內的複合年增長率為 11.61%。市場成長可歸因於監管文獻、科學出版物和臨床研究的增加,對生成式人工智慧的日益依賴,以及對將新技術融入各種醫療流程以簡化重複性任務和減少人為錯誤發生的日益重視。
全球監管機構對人工智慧輔助文件的容忍度正在逐漸提高,前提是能夠維護人工審核並保留審計線索。人工智慧也能確保提交內容各部分的一致性,即使涉及多位作者,也能幫助團隊維護文件的完整性。日益普及的人工智慧平台為臨床文件提供即插即用的解決方案,加速了中型合約研究組織 (CRO) 和製藥公司的採用,這些公司需要在緊迫的期限內完成工作,而無需擴充寫作團隊。透過使用與電子資料擷取 (EDC) 和臨床試驗主文件 (TMF) 系統整合的人工智慧工具,公司可以實現從源頭到提交的資料流自動化。
隨著各種人工智慧工具在醫學寫作中的認知度和接受度不斷提高,世界各地的人工智慧公司正致力於推出新的模型,以提供研究支持並轉變科學內容創作的工作流程。例如,AINGENS, LLC 於 2024 年 11 月推出了 MACg(醫學事務內容產生器),這是一款由人工智慧驅動的醫學寫作工具,提供引文支援、編輯和參考文獻管理。
全部的市場區隔,成為對象的全部的地區和被國家成為對象的全部的地區和被國家提供。
以上公司並非依市佔率排序,且可能根據分析過程中收到的資訊而有所變動。
Global AI in medical writing market is projected to witness a CAGR of 11.61% during the forecast period 2025-2032, growing from USD 845.42 million in 2024 to USD 2035.05 million in 2032. The market's growth can be attributed to the increasing production of regulatory documents, scientific publications, and clinical studies, rising reliance on generative AI, and growing focus on the incorporation of new technologies in different healthcare processes to streamline repetitive tasks and reduce incidences of human error.
Regulatory authorities across the globe are gradually showing openness to AI-assisted documentation, provided that human review is maintained and audit trails are preserved. AI also ensures consistency across sections of a submission, helping teams maintain document integrity even when multiple authors are involved. The growing availability of AI platforms offering plug-and-play solutions for clinical documentation has accelerated adoption among mid-sized CROs and pharmaceutical companies that need to meet tight deadlines without expanding writing teams. By using AI tools that are integrated with electronic data capture (EDC) and trial master file (TMF) systems, companies can automate the flow of data from source to submission.
Due to the increasing awareness and acceptance of different AI tools in medical writing, AI companies across the globe are focusing on launching new models that offer research assistance and are transforming scientific content creation workflow. For instance, in November 2024, AINGENS, LLC introduced the Medical Affairs Content Generator (MACg), an AI-powered medical writing tool that provides citation support, editing, and reference management.
Increasing Investments in AI-Powered Solutions Bolster Market Growth
Substantial investments in AI technologies by pharmaceutical, biotech, and contract research organizations (CROs) are propelling the growth of the market. Companies are increasingly allocating budgets to deploy AI-based platforms that support medical writing, as part of broader digital transformation strategies. With the rising need for multilingual medical documentation and region-specific compliance requirements, global pharmaceutical companies are investing in AI systems capable of handling linguistic and regulatory diversity. Furthermore, AI-based automation enables scalable solutions that can handle the rising volume of documentation stemming from expanding pipelines and increasing post-marketing surveillance needs. The resulting efficiencies are fostering a culture of innovation in regulatory writing and increasing accessibility to medical writing support even among emerging biotech and pharmaceutical companies.
Leading AI companies across the globe are focusing on securing funding to support medical writers in keeping up with new drug launches. For instance, in November 2024, Biolevate raised approximately USD 6.8 million in seed funding to develop solutions that help medical writers keep pace with therapeutic product launches. Such launches are expected to reduce the administrative workload associated with the creation of documents for regulatory bodies, enhancing the efficiency of pharmaceutical professionals, thus providing lucrative growth opportunities for the market.
New Launches Support Market Expansion
Innovations and new launches are allowing biotech and pharmaceutical companies to effectively draft essential documents with the help of sophisticated AI technology. New technologies leverage machine learning and natural language processing to ensure compliance with regulatory standards, enhancing consistency and accuracy in medical content and minimizing human errors. The integration of AI tools is also able to address the increasing complexity of regulatory processes and clinical research, allowing companies to adapt to the digital transformation trends and the evolving requirements of the industry.
The key players in the market are focusing on launching new solutions for industrial applications. For instance, in February 2025, Indegene Inc. launched Cortex, a generative AI platform designed for the life science industry. The platform plays a crucial role in scaling and developing high-value life science applications, including improving the efficiency of medical writing and optimization of the content supply chain. By leveraging large language models, the platform delivers accurate and reliable results, with better ROI and faster turnaround times.
Clinical Writing Witnesses Fastest Growth
The increasing volume and complexity of clinical trial data along with the stringent regulatory requirements is propelling the requirement for consistent and accurate documentation. As of 23rd May 2025, 538,875 studies are registered at ClinicalTrials.gov, the publicly available registry and results database, that is run by the National Library of Medicine (NLM) at the National Institutes of Health (NIH).
AI tools are well-suited for addressing the rising requirements for automation of repetitive tasks including report generation and summarization, improving turnaround time, and reducing human error. Furthermore, advancements in machine learning and natural language processing are making AI tools more suitable for handling specialized language requirements of clinical writing. As healthcare and pharmaceutical companies across the globe recognize the benefits of AI in managing clinical documentation, including improved accuracy and efficiency and economic benefits, adoption rates are increasing, propelling the market's demand.
North America Holds Major Market Share
The region's dominance in the market can be attributed to the presence of a favorable regulatory environment, strong presence of pharmaceutical companies, and easy acceptance of new technologies. Health Canada and the United States Food and Drug Administration (FDA) are both acknowledging the potential of AI in medical writing and healthcare documentation, supporting the market's expansion in the region.
Furthermore, the increasing shortage of skilled medical writers in the region is encouraging companies to actively invest in AI and launch now AI-integrated solutions to tackle complex documents and manage the increased workload. For instance, in July 2024, InSilico Medicine launched DORA, an AI assistant for drafting research papers. The AI assistant uses large language models to draft case studies and academic papers, in addition to patents and grants. Such launches are expected to boost productivity and reduce barriers for research professionals with limited resources.
Future Market Scenario (2025-2032F)
The market is expected to witness strong growth opportunities in the coming years owing to the rising complexity of regulatory frameworks and the increasing volume of clinical data. Advancements in generative AI and language models are expected to improve the narrative quality and contextual understanding of AI-written documents. Leading market players are focusing on launching domain-specific AI solutions that cater to diverse therapeutic areas. Furthermore, regulatory bodies across the globe are working on introducing new guidelines for the ethical use of AI in medical writing. Over the period, AI tools are anticipated to not only support content generation but also aid in optimizing submission strategies, ensuring standardization in global documentation processes.
Key Players Landscape and Outlook
The key players in the market are focusing on technological innovations and the integration of generative AI with their regulatory writing software. For instance, in June 2024, Certara, Inc. launched its CoAuthor regulatory writing software for medical writers. The software combines structured content authoring tools, document templates, and generative AI to accelerate the creation of regulatory documents. Such innovations are improving quality, consistency, and efficiency in medical writing by reducing drafting time. This integration allows Certara to strengthen its position in the market by allowing scientists and healthcare professionals to manage regulatory demands and tackle increasing data complexities, thus providing lucrative growth opportunities for the market.
All segments will be provided for all regions and countries covered
Companies mentioned above DO NOT hold any order as per market share and can be changed as per information available during research work.