市場調查報告書
商品編碼
1280657
藥物警戒市場——按類型(軟件、服務(按流程、按活動(自發報告、增強的不良事件報告、隊列事件監測)、臨床試驗階段、服務提供商、最終用途、預測,2023-2032 年Pharmacovigilance Market-By Type (Software, Service {By Process, By Activity [Spontaneous Reporting, Intensified Adverse Drug Reaction Reporting, Cohort Event Monitoring]}), By Clinical Trial Phase, Service Provider, By End-use, & Forecast, 2023-2032 |
全球藥物警戒市場將從 2023 年增長到 2032 年,這得益於對藥物警戒不斷增長的需求以及對數據驅動洞察力的需求,以確保患者安全,預計將出現顯著增長。
此外,隨著嚴格的藥品審批監管要求,對新藥和創新藥的需求不斷增加,預計將推動未來十年的市場增長。
藥物不良反應 (ADR) 和藥物毒性發生率的上升推動了對藥物警戒的需求。 由於這些療法的種類和可用性不斷增加,必須密切監測它們的安全性和有效性。 藥物警戒對於確保藥物的益處超過可能的風險的重要性推動了產品的採用。 此外,全球人口的持續激增和慢性病患病率的上升也推動了對藥物安全的需求。 根據疾病預防控制中心的數據,每年約有 877,500 名美國人死於心髒病。
疾病負擔的增加以及更多專注於有前途的合作夥伴關係和合併以引領行業的主要市場參與者將有利於市場增長。 例如,2023 年 4 月,德國製藥公司 PharmaLex 宣布與澳大利亞和新西蘭藥物警戒提供商 Cpharm 進行戰略合併。 通過這種合作關係,兩家公司的目標是在澳大利亞市場提供端到端的解決方案,並擴大他們的醫療服務和客戶群。
藥物警戒市場在類型、臨床試驗階段、服務提供商、最終用途和地區方面存在分歧。
根據臨床試驗階段,到 2032 年底,2 期部分預計將達到 4.1 億美元以上。 將進行第二階段試驗,以評估候選藥物在大量患有相關疾病或病症的患者中的安全性和有效性。 全球範圍內越來越多的臨床試驗增加了對強大的藥物警戒系統的需求,以在這些試驗期間監測和確保患者安全。
就最終用途而言,醫療器械公司細分市場的藥物警戒市場價值到 2022 年將超過 25 億美元。 藥物警戒服務提供商為公司提供醫療器械安全概況,從處理和報告單個不良事件到將產品撤出市場作為現場安全糾正措施的一部分。 監管機構越來越關注醫療器械的上市後監督和安全監測,這推動了產品的採用。
預計從 2023 年到 2032 年,亞太地區的藥物警戒市場將呈現出驚人的複合年增長率。 這是由於大量的外包機構。 生產力、成本效率和資源共享的提高預計將在未來幾年增加區域對藥物警戒的需求。 此外,人口基數的擴大以及藥物攝入量和醫療保健需求的增加也補充了該地區的市場增長。
Global Pharmacovigilance Market is expected to showcase remarkable growth over 2023-2032, driven by the increasing demand for drug safety monitoring and the need for data-driven insights to ensure patient safety. In addition, increasing demand for new and innovative drugs, in line with stringent regulatory requirements for drug approval, will fuel market growth over the next ten years.
The rising incidence rate of adverse drug reactions (ADR) and drug toxicity is encouraging the demand for pharmacovigilance. The safety and effectiveness of these treatments need to be closely monitored, given their increasing diversity and availability. The importance of pharmacovigilance in ensuring that the advantages of medicines outweigh any possible hazards is pushing product adoption. Moreover, the consistent surge in the global population and increased prevalence of chronic diseases have also propelled the need for drug safety. According to CDC, around 877.500 Americans die of heart strokes each year.
The growing disease burden and the increasing focus of key market players on promising partnerships and mergers to stay ahead in the industry will favor market growth. For instance, in April 2023, PharmaLex, a German pharmaceutical firm, announced a strategic merger with Cpharm, a pharmacovigilance provider in Australia and New Zealand. With this alliance, the companies aim to offer end-to-end solutions in the Australian market and expand their medical services & customer base.
The pharmacovigilance market is bifurcated in terms of type, clinical trial phase, service provider, end-use, and region.
Based on the clinical trial phase, the phase 2 segment is expected to reach over $410 million by the end of 2032. This second stage of trials is conducted to evaluate the safety and efficacy of a drug candidate in a larger group of patients with the target disease or condition. The rising number of clinical trials worldwide is fueling the need for robust pharmacovigilance systems to monitor and ensure patient safety during these trials.
With respect to end-use, the pharmacovigilance market value from the medical device companies segment was over $2.5 billion in 2022. Pharmacovigilance service providers supply medical device safety profiles to companies, ranging from the processing and reporting of single adverse incidents through the withdrawal of products from the market as part of a Field Safety Corrective Action. The greater emphasis of regulatory bodies on post-market surveillance and safety monitoring of medical devices is bolstering product uptake.
Asia Pacific pharmacovigilance market is expected to exhibit an appreciable CAGR between 2023 and 2032, attributed to the availability of numerous outsourcing organizations. The increasing productivity, cost efficiency, and resource sharing are expected to drive regional demand for pharmacovigilance in the upcoming years. Additionally, the expanding population base with increased drug intake and healthcare demand are also complementing the regional market growth.