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市場調查報告書
商品編碼
1373796
全球學名藥市場 - 市場規模、佔有率、成長分析:按品牌、給藥途徑- 產業預測(2023-2030)Global Generic Drugs Market Size, Share, Growth Analysis, By Brand (Pure and Branded), By Route(Administration, including oral) - Industry Forecast 2023-2030 |
2021年全球學名藥市場規模為4168.6億美元,預計在預測期內(2023-2030年)年複合成長率為5.4%,從2022年的4393.7億美元成長到6692億美元2030年。
由於品牌藥物專利到期、醫療成本上升以及對更便宜的治療方案的需求等因素,全球學名藥市場正在經歷顯著成長。這種成長的關鍵促進因素是許多重磅藥物的專利已經到期,使得學名藥製造商能夠競爭並以更低的價格提供基本藥物。雖然慢性病的增加進一步增加了對具有成本效益的治療方案的需求,但各國政府的政策和醫療保健舉措,特別是在新興經濟體,正在增加學名藥的可及性並降低醫療保健成本。我們的目標是減少這種情況。簡化藥物核准流程和法律規範的配合措施也正在推動市場擴張。然而,全球學名藥市場也面臨挑戰。
心血管疾病、糖尿病、呼吸系統疾病和癌症等慢性疾病在全球範圍內的罹患率不斷上升,刺激了對具有成本效益的治療方案的需求,從而導致對學名藥市場的需求增加。
各國政府正在製定政策並發起計劃,以增加學名藥的使用,其總體目標是降低醫療保健成本、改善關鍵藥物的獲取以及促進學名藥的採用。這些策略涉及學名藥替代和價格法規機制。
學名藥行業面臨著多方面且苛刻的法規環境,學名藥製造商必須通過複雜的核准流程,需要證明與品牌藥的生物等效性。是的。這些法規障礙可能會阻礙學名藥進入市場並增加製造商的成本。
該報告考察了全球學名藥市場,並提供了市場概況,包括按品牌、給藥途徑、地區和參與市場的公司概況分類的趨勢。
Global Generic Drugs Market size was valued at USD 416.86 Billion in 2021 and is poised to grow from USD 439.37 Billion in 2022 to USD 669.20 Billion by 2030, at a CAGR of 5.4% during the forecast period (2023-2030).
The global generic drugs market has seen remarkable growth due to factors like patent expirations of branded medications, rising healthcare expenses, and the need for more affordable treatment choices. This growth is primarily driven by the expiration of patents for many blockbuster drugs, enabling generic drug manufacturers to compete and offer lower-cost essential medications. The increasing prevalence of chronic diseases has further boosted the demand for cost-effective treatment options, while government policies and healthcare initiatives in various countries aim to enhance accessibility to generic drugs and reduce healthcare costs, particularly in emerging economies. Efforts to streamline drug approval processes and regulatory frameworks have also facilitated market expansion. However, the global generic drugs market encounters certain challenges.
Top-down and bottom-up approaches were used to estimate and validate the size of the global generic drugs market and to estimate the size of various other dependent submarkets. The research methodology used to estimate the market size includes the following details: The key players in the market were identified through secondary research, and their market shares in the respective regions were determined through primary and secondary research. This entire procedure includes the study of the annual and financial reports of the top market players and extensive interviews for key insights from industry leaders such as CEOs, VPs, directors, and marketing executives. All percentage shares split, and breakdowns were determined by using secondary sources and verified through Primary sources. All possible parameters that affect the markets covered in this research study have been accounted for, viewed in extensive detail, verified through primary research, and analyzed to get the final quantitative and qualitative data.
Segments covered in this report
The global generic drugs market is segmented on the basis of brand, route, and region. By brand, the market is segmented into pure generic drugs and branded generic drugs. By route, the market is segmented into administration, including oral, topical, parental (injectable), and others (such as inhalation, nasal, and ophthalmic). By region, the market is segmented into North America, Europe, Asia Pacific, Middle East and Africa, and Latin America.
Drivers:
Increasing Chronic Diseases
The increasing worldwide incidence of chronic illnesses, including cardiovascular ailments, diabetes, respiratory issues, and cancer, is fueling the demand for cost-effective treatment options, leading to a rising market demand for generic drugs.
Government Initiatives
In numerous nations, governments are enacting policies and launching initiatives designed to encourage the utilization of generic medications, with the overarching goals of decreasing healthcare costs, enhancing access to vital drugs, and boosting generic drug adoption. These strategies involve mechanisms such as generic substitution and pricing regulations.
Restraints:
Complex Regulatory Environment
The generic drugs industry confronts a multifaceted and demanding regulatory environment, where generic drug producers must adeptly traverse intricate approval procedures that necessitate the demonstration of bioequivalence with branded medications. These regulatory hurdles have the potential to impede the market introduction of generic drugs and escalate expenses for manufacturers.
Perception and Trust Issues
Ensuring broader acceptance and adoption of generic drugs requires addressing the apprehensions of both patients and healthcare providers regarding the quality, effectiveness, and safety of generic medications when compared to their brand-name equivalents. To achieve this, it is imperative to establish trust and educate all stakeholders about the comparable quality and cost-effectiveness of generic drugs.
Market Trends:
Market consolidation in the pharmaceutical industry is on the rise, characterized by larger pharmaceutical companies either acquiring smaller generic drug manufacturers or forging strategic partnerships. This consolidation strategy is geared towards broadening product offerings, bolstering manufacturing capacities, and strengthening market presence.
There is a growing emphasis on biosimilars, generic versions of biologic drugs, as they gain momentum in both development and commercialization. These biosimilars are gaining significance in the worldwide generic drugs market by providing affordable alternatives to costly biologics.