Pharmaceutical Contract Manufacturing

Pharmaceutical Contract Manufacturing

Global Pharmaceutical Contract Manufacturing Market to Reach US$159.8 Billion by 2030

The global market for Pharmaceutical Contract Manufacturing estimated at US$112.4 Billion in the year 2023, is expected to reach US$159.8 Billion by 2030, growing at a CAGR of 5.2% over the analysis period 2023-2030. API/Bulk Drugs, one of the segments analyzed in the report, is expected to record a 4.9% CAGR and reach US$94.8 Billion by the end of the analysis period. Growth in the Advanced Drug Delivery Formulations segment is estimated at 4.4% CAGR over the analysis period.

The U.S. Market is Estimated at US$33.9 Billion While China is Forecast to Grow at 6.4% CAGR

The Pharmaceutical Contract Manufacturing market in the U.S. is estimated at US$33.9 Billion in the year 2023. China, the world`s second largest economy, is forecast to reach a projected market size of US$27.2 Billion by the year 2030 trailing a CAGR of 6.4% over the analysis period 2023-2030. Among the other noteworthy geographic markets are Japan and Canada, each forecast to grow at a CAGR of 4.0% and 4.6% respectively over the analysis period. Within Europe, Germany is forecast to grow at approximately 4.8% CAGR.

Global Pharmaceutical Contract Manufacturing Market - Key Trends & Drivers Summarized

What Is Pharmaceutical Contract Manufacturing, and Why Is It Essential?
Pharmaceutical contract manufacturing involves outsourcing the production of pharmaceutical products to third-party organizations. This business model allows pharmaceutical companies to focus on their core competencies such as drug discovery, development, and marketing, while contract manufacturers (CMOs) handle the complexities of production, including compliance with stringent regulatory standards. This partnership is crucial for small and mid-sized biotech firms that may lack the infrastructure or capital to invest in manufacturing facilities. Moreover, even large pharmaceutical companies leverage this model to enhance flexibility, manage costs, and reduce time to market for new medications.

How Are Global Regulations Shaping the Market?
Regulatory compliance is a pivotal aspect of pharmaceutical contract manufacturing, with stringent guidelines set by authorities like the FDA (U.S. Food and Drug Administration), EMA (European Medicines Agency), and other global regulatory bodies. These regulations ensure that pharmaceutical products are consistently produced and controlled to quality standards. Contract manufacturers must adapt to these evolving regulations, which often involve substantial investments in technology and processes to ensure compliance. As regulatory pressures increase, pharmaceutical companies are increasingly relying on CMOs that can navigate complex regulatory landscapes, thus ensuring the safety, efficacy, and quality of pharmaceutical products.

What Technological Advances Are Impacting Contract Manufacturing?
Technological advancements are profoundly transforming pharmaceutical contract manufacturing. Innovations such as continuous manufacturing, which streamlines production and improves efficiency, are becoming more prevalent. Automation and robotics have also been widely adopted to enhance precision and reduce human error in production processes. Additionally, advanced analytics and real-time monitoring systems are being implemented to ensure quality control throughout the manufacturing process. These technologies not only improve product quality but also reduce waste and enhance scalability, making the production process more cost-effective and efficient.

What Drives the Growth in the Pharmaceutical Contract Manufacturing Market?
The growth in the pharmaceutical contract manufacturing market is driven by several factors, including the rising demand for generic medicines, the increasing complexity of drug production, and the expansion of the biologics market. As patent cliffs lead to increased generic competition, pharmaceutical companies are turning to CMOs to expedite production and capitalize on market opportunities. The complexity of producing new generations of drugs, especially biologics and personalized medicines, also necessitates specialized capabilities that many pharmaceutical firms find more feasible to outsource. Additionally, the shift towards personalized medicine is pushing companies to adapt to flexible and scalable production processes, which contract manufacturers are equipped to handle. These trends, combined with the global push for cost efficiency and faster time-to-market, continue to drive significant growth in this sector, highlighting its critical role in the pharmaceutical industry’s supply chain.

Select Competitors (Total 192 Featured) -

• AbbVie Inc.
• Aenova Holding GmbH
• Catalent Inc.
• Enteris BioPharma, Inc.
• Jubilant Pharma Ltd.
• Kemwell Biopharma Pvt. Ltd.
• Lifecore Biomedical
• Lonza Group Ltd.
• Thermo Fisher Scientific, Inc.
• WuXi AppTec Co., Ltd.

Please note: Reports are sold as single-site single-user licenses. Electronic versions require 24-48 hours as each copy is customized to the client with digital controls and custom watermarks. The Publisher uses digital controls protecting against copying and printing is restricted to one full copy to be used at the same location.

The latest version of Adobe Acrobat Reader is required to view the report. Upon ordering an electronic version, the Publisher will provide a link to download the purchased report.

Prior to fulfillment of an order, the client will be required to sign a document detailing the purchase terms for a publication from this publisher.