The global viral inactivation market value was USD 615.8 million in 2022, driven by the need to eliminate viral contaminants from biopharmaceutical products across the globe. The market size is anticipated to grow at a CAGR of 11.5% during the forecast period of 2023-2031 to achieve a value of USD 1640 million by 2031.
Advancements in viral inactivation technologies are shaping the market, with ongoing research and development efforts focused on improving the efficacy, efficiency, and safety of viral inactivation methods. Innovative approaches such as advanced filtration techniques, non-thermal plasma treatment, and novel chemical agents are being explored to enhance the viral inactivation process. These advancements aim to provide robust and reliable viral inactivation while minimizing the impact on product quality and efficacy.
The market for viral inactivation also benefits from the integration of continuous manufacturing processes. Continuous manufacturing offers advantages such as improved process efficiency, reduced costs, and enhanced product quality control. Integrating viral inactivation within continuous manufacturing platforms enables real-time monitoring and control of the viral inactivation process, leading to streamlined production and reduced risks of contamination.
Introduction
Viral inactivation is a critical process used in the manufacturing of biopharmaceutical products to ensure the elimination or inactivation of viruses present in biological materials. It involves the application of various physical or chemical methods to reduce the infectivity of viruses without significantly impacting the therapeutic properties of the product. Viral inactivation plays a crucial role in ensuring the safety of biologics, vaccines, and other therapeutic products by minimizing the risk of viral transmission to patients.Key Trends in the Viral Inactivation Market
Some of the key trends in the market are:- Increasing Regulatory Requirements: Regulatory authorities continue to strengthen the guidelines and requirements for viral inactivation in biopharmaceutical manufacturing. There is a growing emphasis on comprehensive and effective viral inactivation methods to mitigate the risk of viral contamination. This trend is driven by the need to safeguard patient safety and ensure the quality and efficacy of therapeutic products
- Advancements in Viral Inactivation Technologies: The field of viral inactivation is experiencing continuous advancements in technologies and methods used to inactivate viruses. Newer and more efficient techniques, such as solvent-detergent treatment, heat treatment, irradiation, and filtration, are being developed and optimized to enhance viral inactivation efficacy. These advancements aim to improve the overall safety profile of biopharmaceutical products by providing robust and reliable viral inactivation
- Focus on Viral Safety in Emerging Therapies: With the emergence of novel therapeutic approaches, such as gene therapy and cell-based therapies, there is an increased focus on viral safety in these advanced treatment modalities. These therapies often involve the use of viral vectors or genetically modified cells, making viral inactivation a critical step in the manufacturing process. The development of specialized viral inactivation strategies specific to these advanced therapies is a key trend in the field
- Application of Innovative Technologies: The industry is witnessing the application of innovative technologies in viral inactivation, including the use of nanotechnology, photodynamic therapy, and plasma treatment. These technologies offer the potential for enhanced viral inactivation efficacy while minimizing the impact on product quality. The exploration and adoption of such innovative approaches contribute to the advancement of viral inactivation methods
- Integration of Viral Inactivation in Continuous Manufacturing: Continuous manufacturing is gaining momentum in the biopharmaceutical industry, and there is a growing interest in integrating viral inactivation processes within continuous manufacturing platforms. This integration aims to streamline production, reduce costs, and ensure consistent and efficient viral inactivation throughout the manufacturing process
Viral Inactivation Market Segmentations
Market by Product
- Kits and Reagents
- Services
- Viral Inactivation Systems and Accessories
Market by Application
- Vaccines and Therapeutics
- Stem Cell Products
- Blood and Blood Products
- Tissue and Tissue Products
- Cellular and Gene Therapy
Market by End User
- Pharmaceutical and Biotechnology Companies
- CROs
- Academic and Research Institutes
- Others
Market Breakup by Region
North America
- United States of America
- Canada
Europe
- United Kingdom
- Germany
- France
- Italy
- Others
Asia Pacific
- China
- Japan
- India
- ASEAN
- Australia
- Others
Latin America
- Brazil
- Argentina
- Mexico
- Others
Middle East and Africa
- Saudi Arabia
- United Arab Emirates
- Nigeria
- South Africa
- Others
Viral Inactivation Market Scenario
The market is driven by the increasing need to eliminate viral contaminants from biopharmaceutical products and minimize the risk of viral transmission to patients. Regulatory authorities impose stringent guidelines and requirements for viral inactivation, necessitating the use of effective and validated viral inactivation methods. Biopharmaceutical companies invest in viral inactivation technologies and services to comply with these regulations and deliver high-quality products to the market.Advancements in viral inactivation technologies are shaping the market, with ongoing research and development efforts focused on improving the efficacy, efficiency, and safety of viral inactivation methods. Innovative approaches such as advanced filtration techniques, non-thermal plasma treatment, and novel chemical agents are being explored to enhance the viral inactivation process. These advancements aim to provide robust and reliable viral inactivation while minimizing the impact on product quality and efficacy.
The market for viral inactivation also benefits from the integration of continuous manufacturing processes. Continuous manufacturing offers advantages such as improved process efficiency, reduced costs, and enhanced product quality control. Integrating viral inactivation within continuous manufacturing platforms enables real-time monitoring and control of the viral inactivation process, leading to streamlined production and reduced risks of contamination.
Viral Inactivation Market: Competitor Landscape
The key features of the market report include patent analysis, grants analysis, clinical trials analysis, funding and investment analysis, partnerships, and collaborations analysis by the leading key players. The major companies in the market are as follows:- Rad Source Technologies Inc
- Merck KGaA
- Parker Hannifin Corp
- Sartorius AG
- Cerus Corporation
- Cytiva (Danaher Corporation)
- Charles River Laboratories
- CONVATEC GROUP PLC
- WuXi AppTec
- TERUMO BCT, INC
- Thermo Fisher Scientific Inc
- SCI Automation
Table of Contents
1 Preface2 Report Coverage - Key Segmentation and Scope4 Key Assumptions7 Opportunities and Challenges in the Market15 Value Chain Analysis17 Key Trends and Developments in the Market
3 Report Description
5 Executive Summary
6 Snapshot
8 Global Viral Inactivation Market Analysis
9 North America Viral Inactivation Market Analysis
10 Europe Viral Inactivation Market Analysis
11 Asia Pacific Viral Inactivation Market Analysis
12 Latin America Viral Inactivation Market Analysis
13 Middle East and Africa Viral Inactivation Market Analysis
14 Market Dynamics
16 Competitive Landscape
Companies Mentioned
- Rad Source Technologies Inc
- Merck KGaA
- Parker Hannifin Corp
- Sartorius AG
- Cerus Corporation
Methodology
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Table Information
Report Attribute | Details |
---|---|
No. of Pages | 140 |
Published | May 2023 |
Forecast Period | 2023 - 2031 |
Estimated Market Value ( USD | $ 686.6 Million |
Forecasted Market Value ( USD | $ 1640 Million |
Compound Annual Growth Rate | 11.5% |
Regions Covered | Global |
No. of Companies Mentioned | 5 |