Biologics Contract Manufacturing Markets, 2035: Partnerships Drive Progress: Biopharma CDMO/Biopharma CMO/Biologics Manufacturing Sees Over 61% Increase in Partnerships Post-COVID-19

DUBLIN, Feb. 16, 2024 /PRNewswire/ -- The "Global Biologics Contract Manufacturing (Biopharma CDMO/Biopharma CMO/Biologics Manufacturing) Market 2022-2035 by Type of Service(s) Offered, Type of Biologic Manufactured, Type of Expression System Used, Scale of Operation, Company Size, and Key Geographical Regions" report has been added to ResearchAndMarkets.com's offering.

The global biologics contract manufacturing market is estimated to reach over $19 billion in 2023 and is expected to grow at a compound annual growth rate (CAGR) of ~9% during the forecast period.

One of the primary objectives of the presented market report is to conduct a comprehensive market forecast analysis, aiming to estimate both the current market size and the future opportunities within the biopharmaceutical contract manufacturing sector over the next decade. Drawing insights from various parameters, anticipated adoption trends, and validated through primary research, the report offers an informed estimate of the market's evolution throughout the forecast period from 2023 to 2035.

The biologics contract manufacturing market, also known as the biopharmaceutical CMO market, is a dynamic and rapidly growing sector with a large number of players investing in research and development activities for developing new modalities, such as antibody drug conjugates, biosimilars, and cell and gene therapies. With the increased interest and gradual shift of investment from small molecule drugs to biologics, over the years, more than 250 biologic therapies and vaccines have been developed globally.

Notably, biologics have higher success rates than conventional small-molecule drugs owing to lesser off-target toxicity of biologics, which is one of the key reasons of failures in small molecule drugs development. Given the ongoing scientific advancements and the rise of FDA-approved biologics, the pharmaceutical industry seems to be approaching the era of biologics. In fact, biopharmaceuticals are anticipated to play a significant role in shaping the pharmaceutical industry and will eventually serve as an integral part of traditional medicines.

Moreover, the exuberant development of biologics has revolutionized the treatment of a range of therapeutic conditions, which has further contributed to the exponential growth in the current demand for biologic therapies. It is worth highlighting that numerous biologics manufacturers, including biologics CMOs, have adopted digital technologies in order to enhance their productivity and reliability of existing biologics related processes and facilities. 

However, the complexity of biologics, as well as the integration of emerging technologies, offer challenges for current good manufacturing practices (cGMP) for biologics. Some of the key concerns of contemporary innovators include rate of attrition of pipeline drugs / therapies, long development timelines, current facility limitations, regulatory and compliance-related issues, and inconsistencies related to the quality attributes of the final product.

As a result, an increasing number of biopharmaceutical drug developers are relying on contract manufacturers that are well-equipped with expertise and advanced technologies for their GMP-based manufacturing requirements. These service providers offer end-to-end solutions, including bioprocess development and optimization, to shorten operational timelines and reduce the high costs associated with the production of complex biologic drugs.

In addition, there are some manufacturers that particularly outsource various operations to tap into sophisticated facilities and know-how, particularly if contract manufacturing firms are utilizing cutting-edge technologies, such as software-driven robotics, to enhance manufacturing processes and mitigate the risks and constraints associated with manual methods. With outsourcing becoming increasingly accepted as a viable and beneficial business model within this field, the global market for biologics contract manufacturing is expected to witness remarkable growth during the forecast period.

This comprehensive report provides an in-depth analysis of the current landscape, market size, and future opportunities within the biologics contract manufacturing market for the forecast period. It sheds light on the contributions of various stakeholders in this rapidly evolving segment of the pharmaceutical industry. 

Future Of The Biopharmaceutical CMO Market

• Outsourcing Activities to Witness Significant Growth in the Coming Years
• Shift from One-time Contracts to Strategic Partnerships
• Integration / Adoption of New and Innovative Technologies
• Focus on Niche Therapeutic Areas
• Growing Biosimilars Market to Contribute to the Growth of the Contract Services Segment
• Capability Expansion by CMOs to become One-Stop-Shops
• Offshoring Outsourcing Activities to Maximize Profits and Expand Existing Capacities
• Increase in Financial Inflow and Outsourcing Budgets
• Challenges Faced by Sponsors and Service Providers

Growing Demand for Biologics

• Biologics, mimicking biomolecules in the human body, offer targeted treatment with fewer side effects compared to conventional drugs. This specificity makes them highly sought after in the pharmaceutical and biotechnology sectors.
• Novel modalities like recombinant proteins, vaccines, and cell and gene therapies are gaining traction, positioning biologics to surpass small molecules in revenue.

Fundamental Advancements in Biopharmaceutical Manufacturing

• Single-use technologies have revolutionized biopharmaceutical manufacturing, facilitating rapid process development, particularly during the COVID-19 pandemic.
• Closed plug-and-play solutions allow for process intensification and continuous manufacturing, making them preferable for both developmental phases and commercial production.

Competitive Landscape of Biologics Contract Manufacturing Companies

• The market features over 305 biologics contract manufacturing organizations (CMOs), indicating a surge in demand for manufacturing capacities.
• Notable players offering contract manufacturing services include 3P Biopharmaceuticals, Celltrion, Lonza, and Samsung Biologics, among others.

Biologics Contract Manufacturing Market Size: North America Leading

• The global market for biologics contract manufacturing is estimated to exceed USD 19 billion in 2023, with North America holding the largest market share (34%).
• Asia-Pacific is expected to witness significant growth during the forecast period, driven by increasing R&D investments and clinical studies.

Mammalian Cell Cultures Preferred for Expression Systems

• Mammalian cell cultures are favored for biopharmaceutical production due to their ability to perform post-translational modifications essential for drug safety and efficacy.
• Productivity enhancements in mammalian cell culture processes have been substantial over the past decade.

Investments in Manufacturing Facilities

• Biologics CMOs are expanding their manufacturing capabilities to accommodate growing demand. This includes the addition of new facilities and advancements in services.
• Recent investments by Enzene Biosciences and Biose highlight the industry's commitment to expanding drug development and manufacturing capabilities.

Market Trends Analysis: Increasing Partnerships and Collaborations

• Partnerships and collaborations among stakeholders are driving progress and innovation in biopharmaceutical manufacturing.
• More than 61% of recent deals have focused on manufacturing and development of biologics, showcasing the industry's dedication to advancing product offerings.

Leading CMOs in Biologics Contract Manufacturing

• Key players in biologics contract manufacturing include AGC Biologics, Boehringer Ingelheim, Catalent, Lonza, and WuXi Biologics, among others.
• These companies offer a range of manufacturing services and have established global footprints.

Recent Developments

• Recent initiatives, such as partnerships between 3P Biopharmaceuticals and Zhittya Genesis Medicine, and AGC Biologics and Genenta, underscore ongoing trends in the market towards innovation and collaboration.

The opinions and insights presented in the market report were influenced by discussions held with stakeholders in the industry. The report features detailed transcripts of interviews held with the following industry stakeholders:

• Chief Executive Officer, Mid-Sized Company, Scotland
• Chief Executive Officer and Co-Founder, Small Company, Slovenia
• Chief Technical Officer, Large Company, USA
• President and Chief Operating Officer, Mid-Sized Company, China
• Senior Director of Global Strategic Marketing, Large Company, USA
• Senior Director of Commercial Strategy and Market Insights, Large Company, USA
• Global Head of Sales and Marketing and Head of Business Development, Large Company, USA
• Business Development Manager, Small Company, Spain
• Manager Marketing and Sales, Mid-Sized Company, Germany

All actual figures have been sourced and analyzed from publicly available information forums and primary research discussions. Financial figures mentioned in this market report are in USD, unless otherwise specified.

Key Companies Profiled

• AGC Biologics
• Boehringer Ingelheim
• Catalent
• Cell Therapies
• Charles River Laboratories
• FUJIFILM Diosynth Biotechnologies
• KBI Biopharma
• Kemwell Biopharma
• Lonza
• Miltenyi Biotec
• Minaris Regenerative Medicine
• Samsung Biologics
• Sandoz
• Vetter Pharma
• Wuxi Biologics

For more information about this report visit https://www.researchandmarkets.com/r/awivta

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