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Global Pharmaceutical Continuous Manufacturing Market Analysis Report 2023: Regulatory Acceptance Propelling Continuous Manufacturing Investments through Partnerships and In-house Expansions
Dublin, Feb. 24, 2023 (GLOBE NEWSWIRE) -- The "Global Pharmaceutical Continuous Manufacturing Market, Growth Opportunities" report has been added to ResearchAndMarkets.com's offering.
The global pharma industry is slowly shifting its focus from primary care to specialty medicine and rare diseases. To modify research and development (R&D) models to address and adapt to challenges associated with rare, ultra-rare, and specialty diseases, the strategy is changing from being present in a few large segments to many small segments and exploring new disease areas with high unmet needs.
Continuous manufacturing (CM) is a method for manufacturing end-to-end pharmaceutical products on a single, uninterrupted production line. While batch manufacturing requires transporting, testing, and refeeding materials from one process to the next, continuous processes execute all testing, feeding, and processing inline at a single manufacturing site.
CM helps pharma companies significantly speed up the chemistry and manufacturing processes, which can cut down on the overall manufacturing timelines, especially in critical life-saving drugs. To date, the US Food and Drug Administration (FDA) has approved the manufacture of over 7 drugs using continuous processes, which started off from only one product less than 4 years ago.
In 2020 alone, the FDA approved 4 new drugs to be manufactured using CM. Alongside the FDA, health authorities in Canada, Europe, Australia, Japan, Switzerland, and New Zealand have approved CM application for the production of solid oral dosage forms, indicating the growing acceptance of the technology worldwide.
With such nascent technology, the pharma industry has been applying the technique for processes that are off limits for batch processes, which might include toxic reagents, and for scale-up reactions that include electrochemical or photochemical reactions. Implementing technologies, such as process analytical technology (PAT) and digital twins, for improved real-time decision making will allow for the better control of manufacturing processes, including batch and CM.
Considering the large-scale benefits of flexibility and timeline management and a quantifiable reduction in the cost of manufacturing through automated processes and better resource management, CM is expected to witness large-scale adoption in the form of integrated processes.
Furthermore, the ecosystem is currently focused on pharma companies that take the majority share, in terms of setting up facilities. Contract development and manufacturing organizations (CDMOs), however, are slowly expanding their facilities by collaborating with CM platform vendors, with system integrators and automation experts providing additional support in the optimization manufacturing value chain.
In the coming years, as the regulatory and operational benefits become more realized, CDMOs and pharma companies will likely continue enhancing and building their CM capabilities and expertise to remain competitive.
Key Topics Covered:
1. Strategic Imperatives
Why is it Increasingly Difficult to Grow?
The Strategic Imperative
The Impact of the Top 3 Strategic Imperatives on the Pharmaceutical Continuous Manufacturing (CM) Industry
Growth Opportunities Fuel the Growth Pipeline Engine
2. Growth Opportunity Analysis
Scope of Analysis
Segmentation
Market Trend Analysis
Batch Manufacturing versus CM
Benefits of Adopting CM
Vendor Ecosystem
Growth Drivers
Growth Restraints
3. CM Market Scenario
CM-Adoption Timeline (FDA)
Current Market Scenario of CM Growth
CM-Technology Overview
4. Investment Trends - Partnerships and Expansions
Facility Expansions/Acquisitions
Partnerships/Collaborations
5. Growth Opportunity Analysis - Global Pharmaceutical CM Market
Growth Metrics
Forecast Assumptions
Global Pharmaceutical Market
Revenue Forecast
Revenue Forecast Analysis
Regional Perspective
6. Growth Opportunity Analysis - In-house versus Outsourced
Revenue Forecast-In-house versus Outsourced
Percent Revenue Forecast-In-house versus Outsourced
Revenue Forecast Analysis-In-house versus Outsourced
7. Growth Opportunity Analysis - Small Molecules versus Large Molecules
Revenue Forecast-Small Molecules versus Large Molecules
Percent Revenue Forecast-Small Molecules versus Large Molecules
Revenue Forecast Analysis-Small Molecules versus Large Molecules
8. Growth Opportunity Analysis - Drug Substance versus Drug Product
Revenue Forecast-DS versus DP (Large Molecules)
Revenue Forecast-API versus FDF (Small Molecules)
Revenue Forecast Analysis by Segments
9. Growth Opportunity Analysis - Competitor Assessment
Competitive Environment
Key Competitors by Region-End Users
10. Competitor Profiles - CDMOs Providing CM Services
Cambrex Corporation-Overview
SK Biotek-Overview
Corden Pharma-Overview
Patheon (Thermo Fisher Scientific)-Overview
Wuxi Biologics-Overview
Fujifilm Diosynth Biotechnologies-Overview
11. CM-Equipment Manufacturers
12. Growth Opportunity Universe
Growth Opportunity 1-Capability Expansion for CM in APAC
Growth Opportunity 2-Focus on Process Automation for Enhanced Productivity
Growth Opportunity 3-Viral Vector CM for Gene Therapy
13. Next Steps
For more information about this report visit https://www.researchandmarkets.com/r/bwu4id
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