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市場調查報告書
商品編碼
1351099
2030 年生物製藥 CMO 市場預測:按產品、原產地、服務和地區進行的全球分析Biopharmaceutical CMO Market Forecasts to 2030 - Global Analysis By Product (Biologics, Biosimilars and Other Products), Source, Service and By Geography |
根據Stratistics MRC預測,2023年全球生物製藥CMO市場規模將達151.8億美元,預計2030年將達到394.1億美元,預測期內年複合成長率為14.6%。
生物製藥 CMO,通常稱為合約製造組織,是為生物製藥行業的其他企業(包括包裝和藥品製造)提供合約服務的企業。這使得主要的生物製藥公司能夠外包其製造流程,並專注於新藥的開發和行銷。由於缺乏內部生產能力,許多小型生物技術公司透過外包其填充和成品製造要求來避免資本投資。
據印度藥品工業協會(IDMA)稱,截至2021年7月,基本藥物原料(即製藥行業的API)成本已較疫情前水平飆升約140%,給印度醫藥行業帶來了挑戰。工業.馬蘇.
活性藥物原料藥(API) 的生產需求持續成長。這是由於與老化和癌症相關的疾病日益患病、全球學名藥生產能力不斷提高以及生物創新。因此,市場參與企業將重點放在開拓生物原料藥和擴大原料藥產能。因此,預計生物製藥和小分子原料藥領域都有更好的預測,並且這種趨勢預計將在整個預測期內持續下去。
CRO(委外研發機構)由 FDA(食品藥物管理局)定義和管理。 FDA 也有權要求 CRO 直接對其在臨床實驗申請中承擔的申辦者責任負責。 FDA 必須確保臨床實驗正確進行並符合良好臨床實務和協調的標準。嚴格的法律規範和法規是阻礙市場擴張的主要要素之一。
隨著製藥和生物技術公司在合約製造和開發服務上投入更多資金,該行業將繼續擴大。生物製藥受託製造廠商市場預計將出現兩位數成長,中小型 CMO 的成長速度預計將快於大型 CMO。高成長率主要是由於計劃推出的生物製劑管道數量不斷增加。隨著開發中的生物製藥數量不斷增加,對外包服務的需求將大幅增加。
在一定程度上限制市場擴張的主要挑戰包括建立生產設施所需的高昂初期成本以及以更快的速度擴大生物製造所需的額外資本投資。服務本身的複雜性和法律環境都被認為使 CMO 與客戶談判合約變得困難。由於智慧財產權、保固、成本和交貨日期等問題,客戶和 CMO 之間的談判非常困難。
疫情已成為全球重大公共衛生議題。這場大流行的影響最初是在中國發現的,現在已經波及到其他地區。醫療保健行業的收入成長受到顯著影響。然而,全球市場都出現了有利的需求衝擊。成長率的大幅成長主要是由於 CMO 增加了生物製藥合約的分配。在生物製藥領域,隨著COVID-19的影響持續蔓延,我們正專注於開發高效、安全的疫苗來預防感染,並創造和研究新藥物來治療病毒感染者。
由於該行業缺乏專業知識,預計哺乳動物市場在預測期內將成為最大的市場。他們透過類人轉譯後修飾增強複雜蛋白質加工的能力證明了這一點。已經鑒定多種微生物,並且正在利用創造性策略來挖掘它們的潛力。該領域還受益於新的和改進的表達系統的開發、製程監控解決方案的增加、細胞株工程工具、自動篩選技術和拋棄式設備。
合約製造領域預計在預測期內年複合成長率最高。該地區擁有許多 CMO,它們積極為生物製藥公司提供從細胞培養到填充和加工服務等廣泛的端到端服務。客戶產品開發計畫的製造部門也獲得了大量投資。隨著專注於開拓生物製藥市場的新參與企業選擇合約研究服務來尋找新候選化合物,該領域的成長預計將加速。
預計北美在預測期內將佔據最大的市場佔有率。這是由於同一地區存在多個服務提供者。此外,美國核准的產品中很大一部分是由集體生產組織生產的。還有許多中小型生物製藥公司缺乏建造資源齊全的設施所需的資金和資源。結果,集體管理組織和中小企業之間的相互依賴增加,導致市場寡占。
由於聚合物產量高,預計亞太地區在預測期內將維持最高的年複合成長率。全球生物相似藥核准法規缺乏一致性,對該市場造成了重大影響。該地區的強勁成長主要歸功於越來越多的 CMO 在各國開設製造工廠。由於該地區人口眾多以及糖尿病、癌症和其他慢性病等各種疾病的患病不斷上升,預計市場參與者將享有良好的成長預測。
According to Stratistics MRC, the Global Biopharmaceutical CMO Market is accounted for $15.18 billion in 2023 and is expected to reach $39.41 billion by 2030 growing at a CAGR of 14.6% during the forecast period. A biopharmaceutical CMO, often referred to as a contract manufacturing organization, is a business that provides contract services to other businesses in the biopharmaceutical industry, including packaging and drug manufacture. This enables large biopharmaceutical companies to outsource their manufacturing process, allowing them to concentrate on the development and marketing of new drugs. Because they don't have the internal production capacity, many small biotechnology businesses outsource their fill and finish manufacturing requirements, which helps them avoid having to make capital investments.
According to the Indian Drug Manufacturers Association (IDMA), as of July 2021, the cost of raw materials for essential drugs, called APIs in the pharma sector, has seen a steep rise of around 140% since the pre-pandemic levels, posing a challenge for the industry.
The manufacture of Active Pharmaceutical Ingredients (API) is experiencing a constant increase in demand. This is due to an increase in the prevalence of age- and cancer-related disorders, increased worldwide generic production capacities, and biologic innovation. As a result, market participants are concentrating on developing biological APIs and expanding their API production capabilities. Better prospects are anticipated as a result, both in the biopharmaceutical and small molecule API sectors, and it is anticipated that this trend will continue throughout the course of the forecast year.
Contract research organizations (CROs) are defined and governed by the Food and Drug Administration (FDA), which also has the authority to hold CROs directly liable for any sponsor responsibilities they take on in connection with an investigational new drug application. It must guarantee that the drug study is correctly run and complies with the standards for good clinical practice and harmonisation. The strict regulatory framework or rules and regulations are one of the main things that are anticipated to impede market expansion.
As pharmaceutical and biotechnology companies spend more on contract manufacturing and development services, this industry will keep expanding. The market for biopharmaceutical contract manufacturing organizations is predicted to increase by double digits, with smaller CMOs anticipating faster growth than bigger CMOs. The high growth rate is mostly attributable to the expanding number of biologics pipelines that are planned for release. The demand for outsourcing services will be significantly increased by the growth in the number of biopharmaceuticals in development.
The significant challenges limiting the market expansion to some level include the high initial expenditure needed for the creation of manufacturing facilities and investments in additional equipment to start bio manufacturing at a faster rate. The complexity of the service itself and the legal environment have both been recognized to make contract negotiations between CMOs and customers challenging. Because of issues including intellectual property rights, warranties, cost, and timeliness, negotiations between clients and CMOs are difficult.
The pandemic has become a huge public health concern around the world. The pandemic's impacts, which were initially discovered in China, are now being felt elsewhere. The healthcare sector's revenue growth was significantly impacted. But the market saw a favorable demand shock all around the world. The sudden increase in growth rate can be largely attributed to the CMOs' increased allocation of biopharmaceutical contracts. The biopharmaceutical sector is concentrating on the development of efficient and safe vaccinations to prevent infection as the impact of COVID-19 grows, as well as on the creation and research of new medicines to treat those who have been infected with the virus.
The mammalian segment is expected to be the largest during the forecast period owing to the lack of internal expertise in the industry. This is demonstrated by their capacity to enhance complicated protein treatments with post-translational modifications that are human-like. Diverse microorganisms are being identified and their potential is being explored through the use of creative tactics. The segment has also profited significantly from the development of novel and improved expression systems, increased process monitoring solutions, cell line engineering tools, automated screening techniques, and disposable devices.
The contract manufacturing segment is expected to have the highest CAGR during the forecast period. The region is home to a sizable number of CMOs that are actively engaged in offering biopharma companies a wide range of services, including end-to-end coverage from cell cultivation to fill/finish services. The manufacturing component of clients' product development programs is also receiving significant investment. It is projected that new market entrants and small businesses who are focused on the development of biopharmaceuticals will choose contract research services for their discovery programs of new candidates, which will accelerate the segment's growth.
North America is projected to hold the largest market share during the forecast period. This can be attributed to the local presence of several service providers in the region. Furthermore, CMOs produce a sizeable portion of the approved products in the US. Numerous small- and mid-sized biopharmaceutical companies are present, but they lack the funding and resources necessary to build facilities with adequate resources. As a result, the interdependence between CMOs and SMEs has grown, leading to the market's domination.
Asia Pacific is projected to hold the highest CAGR over the forecast period, due to the high volume of large molecule production in this country. The market has been heavily influenced by the lack of global regulatory consistency for biosimilar approval. The region's robust growth is mostly attributable to the rising number of CMOs opening manufacturing facilities across nations. It is projected that the region's high population and rising prevalence of various ailments like diabetes, cancer, and other chronic diseases will present market players with lucrative growth prospects.
Some of the key players in Biopharmaceutical CMO market include: JRS Pharma, Toyobo Co., Ltd., Rentschler Biopharma SE, Inno Biologics Sdn Bhd, Fujifilm Diosynth Biotechnologies U.S.A., Inc., Laboratory Corporation of America Holdings, Biomeva GmbH, Samsung Biologics, ProBioGen AG, Boehringer Ingelheim GmbH, Lonza Group AG, CMC Biologics, ICON Plc, AbbVie Inc. and Thermo Fisher Scientific Inc (Patheon & PPD).
In June 2023, FUJIFILM Corporation announced that it will launch a commercial office*1 in Tokyo to provide enhanced sales support and customer service for Contract Development and Manufacturing services for Biologics and Advanced Therapies to Asia-based pharmaceutical and biotechnology companies.
In June 2023, Lonza to acquired Synaffix and strengthen antibody-drug conjugates offering. Acquisition will further strengthen Lonza's bioconjugates offering through the integration of the industry-leading proprietary Synaffix technology platform and R&D capabilities, including payload and site-specific linker technology
In May 2022, Germany's Boehringer Ingelheim (BI) has announced that it has acquired approval from the Central Drugs Standard Control Organization (CDSCO) to market its medicine Jardiance (empagliflozin) in India, for the whole spectrum of heart failure disorders regardless of ejection fraction.
Note: Tables for North America, Europe, APAC, South America, and Middle East & Africa Regions are also represented in the same manner as above.