The surge in demand for COVID-19 vaccines has presented lucrative opportunities for both innovators and contract service providers having continuous and semi-continuous manufacturing capabilities for biointensification
Given the growing pipeline of biological drugs, and the rising preference for such therapeutic interventions, the demand for cost-effective biomanufacturing processes has increased. As a result, several innovators and contract service providers are evaluating the potential of continuous and semi-continuous upstream and downstream bioprocessing technologies, owing to their various advantages.
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Key Market Insights
Presently, more than 70 companies claim to have capabilities for continuous manufacturing of biologics
Close to 45% of the continuous and semi-continuous bioprocessing companies are headquartered in Europe; further, around 20% of these companies have established their dedicated facilities in other geographical regions, such as North America and Asia-Pacific.
Over 65% of the installed continuous upstream manufacturing capacity belongs to established players
More than 40% of the global continuous upstream processing capacity is installed in Europe, followed by Asia-Pacific (33%). Further, close to 55% of the capacity belongs to the facilities owned by contract service providers.
Continuous and semi-continuous bio-intensification approach has potential to save ~40% of the overall biopharmaceutical manufacturing cost
By 2030, we expect that adoption of continuous and semi-continuous approach is likely to enable the net, annual cost savings of close to USD 50 billion.
By 2030, the opportunity within the continuous and semi-continuous bioprocessing market is likely to be over USD 500 million
Presently, the use of continuous and semi-continuous bio-intensification approach is largely restricted to the developed nations, and the majority of revenues from biologics manufactured via this approach are distributed between North America (~25%) and Europe (~40%). Once this process is adopted for the end-to-end manufacturing of biologics, estimates in the report suggest are likely to grow at even higher pace.
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Key Questions Answered
- Who are the leading contract manufacturers with expertise in continuous and semi-continuous bioprocessing?
- Who are the leading innovators / drug developers with expertise in continuous and semi-continuous bioprocessing?
- In which regions are majority of the continuous and semi-continuous bioprocessing facilities located?
- What is the likely cost saving potential of continuous and semi-continuous bioprocessing technology?
- What is the currently installed global capacity for continuous and semi-continuous bioprocessing?
- How is the current and future market opportunity likely to be distributed across key market segments?
The USD 500+ million (by 2030) financial opportunity associated with continuous and semi-continuous bioprocessing services market has been analyzed across the following segments:
- Type of Manufacturer
- Innovator / Drug Developer
- Contract Service Provider
- Company Size
- Scale of Operation
- Preclinical / Clinical
- Stage of Bioprocess
- Upstream Bioprocessing
- Downstream Bioprocessing
- Geographical Regions
- North America
- Latin America and Rest of the World
The research includes profiles of key players (listed below), featuring a brief overview of the company, financial information (if available), details on its service portfolio, continuous and semi-continuous bioprocessing capabilities, scale of operation, stage of bioprocess, types of biologics manufactured, continuous and semi-continuous bioprocessing manufacturing facilities, recent developments and an informed future outlook.
- AGC Biologics
- Bristol-Myers Squibb
- Enzene Biosciences
- FUJIFLM Diosynth Biotechnologies
- Merck KGaA
- Sanofi Genzyme
- UCB Pharma
- WuXi Biologics
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