NEWARK, Del, March 31, 2023 (GLOBE NEWSWIRE) -- As per the current market research conducted by FMI, the global Bioprocess Validation Market is expected to record a CAGR of 9.20% from 2023 to 2033. In 2023, the market size is projected to reach a valuation of US$ 449.03 million. By 2033, the valuation is anticipated to be worth US$ 996.29 million.
The bioprocess validation market is expected to witness significant growth prospects in the coming years. Bioprocess validation is a critical step in the manufacturing of biologics, including vaccines, gene therapies, and cell therapies. It ensures that the biologics produced are safe, pure, and effective.
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- One of the significant factors driving the growth of the market is the increasing demand for bioprocess validation development to ensure compliance with regulations. Biologics have emerged as a promising area for the treatment of various diseases, and the demand for biologics is expected to continue to grow in the coming years. This, in turn, is expected to drive the demand for bioprocess validation services.
- The growth of the market is driven by the increasing regulatory scrutiny of biologics and bioprocess technology. Regulatory bodies around the world, such as the FDA and EMA, have stringent requirements for the manufacturing of biologics. Bioprocess validation is an essential part of meeting these requirements, and as a result, the demand for bioprocess validation services is expected to continue to grow.
- The advancements in technology are also expected to drive the growth of the market. The development of advanced analytical tools and sensors, as well as the integration of automation and artificial intelligence into bioprocess validation, are expected to improve the efficiency and accuracy of the validation process.
The bioprocess validation market is expected to see significant growth prospects in the coming years due to the increasing demand for biologics, regulatory scrutiny of biologics, and advancements in bioprocess technology.
The United States Market
The bioprocess validation market in the United States is driven by the increasing demand for biologics and biosimilars. The market involves the validation of various bioprocesses used in the pharmaceutical, biotechnology, and life sciences industries, including validation of manufacturing processes, analytical methods, and cleaning procedures.
Recently, the United States Food and Drug Administration (FDA) has placed greater emphasis on the importance of bioprocess validation in ensuring the safety and efficacy of biologics and biosimilars. This has led to increased demand for bioprocess validation services and products in the United States.
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The United Kingdom Market
The rising demand for biologics as well as biosimilars in the biomedical and pharmaceutical sectors, the United Kingdom market for bioprocess validation is expanding steadily.
The United Kingdom is home to numerous biopharmaceutical companies and research institutions that are actively engaged in developing new biologics and biosimilars. These companies require reliable and efficient bioprocess validation techniques to ensure the quality and safety of their products.
One of the significant factors driving the growth of the market in the United Kingdom is the increasing focus on regulatory compliance and quality control in the industry.
The United Kingdom's regulatory authority, the medicines and healthcare products regulatory agency (MHRA) has set strict guidelines and regulations for the manufacturing and validation of biopharmaceutical products, which has led to increased demand for bioprocess validation services and products.
Here are Some Key Takeaways for the Market:
- The market is driven by the increasing demand for biologics and biosimilars, as well as the growing emphasis on regulatory compliance and quality control in the industry.
- The global bioprocess validation market is expected to record a CAGR of 9.20% from 2023 to 2033 to reach US$ 996.29 million by 2033.
- The United States and the United Kingdom are two significant markets for bioprocess validation, with significant growth potential due to the increasing demand for biologics and biosimilars.
- The bioprocess validation market size is anticipated to reach a valuation of US$ 449.03 million in 2023.
Competitive Background:
The key players operating in the market are investing in mergers and acquisitions in order to gain a significant market share. The manufacturers are also investing in research and development, and are introducing innovative methods to boost production capacity. Product development and market expansion are significant aspects of the market. As a result, market participants are likely to have a better overall revenue share in the global market.
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Prominent Key Players
- Thermo Fisher Scientific Inc.
- Sartorius AG
- Eurofins Scientific, Inc.
- Merck KGaA
- Lonza
- Danaher Corporation
- SGS S.A.
- Charles River Laboratories
- Toxikon Corporation
- Cobetter Filtration Equipment Co., Ltd.
Bioprocess Validation Market by Category
By Testing Type:
- Extractables & Leachables Testing
- Bioprocess Residuals Testing
- Viral Clearance Testing
- Filtration & Fermentation Systems Testing
- Others
By Stage:
- Process Design
- Process Qualification
- Continued Process Verification
By Mode:
- In House
- Outsourced
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By Region:
- North America
- Latin America
- Europe
- East Asia
- South Asia
- Oceania
- The Middle East & Africa
Table of Content
1. Executive Summary | Bioprocess Validation Market
1.1. Global Market Outlook
1.2. Demand-side Trends
1.3. Supply-side Trends
1.4. Technology Roadmap Analysis
1.5. Analysis and Recommendations
2. Market Overview
2.1. Market Coverage / Taxonomy
2.2. Market Definition / Scope / Limitations
3. Market Background
3.1. Market Dynamics
3.1.1. Drivers
3.1.2. Restraints
3.1.3. Opportunity
3.1.4. Trends
3.2. Scenario Forecast
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