Roots Analysis has done a detailed study on Biopharma Contract Manufacturing Market (3rd Edition), 2019-2030, covering key aspects of the industry’s evolution and identifying potential future growth opportunities.

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Key Market Insights
 Over 235 companies worldwide claim to offer contract manufacturing services for various types of biopharmaceutical drug / therapy products.
 The market landscape is highly fragmented featuring the presence of both established players and new entrants; majority of biopharmaceutical CMOs are based in the developed geographies.
 Case study: CMOs focusing on niche biologic markets, primarily novel product candidates for which in-house biomanufacturing expertise is low, are likely to experience significant growth in the coming years.
 The installed global contract manufacturing capacity, spread across various geographies, is currently estimated to be over 4.5 million liters.
 The demand for contract manufacturing services is expected to rise across different therapeutic areas; closer inspection of available capacity and expected utilization trend are required to optimize supply parameters.
 With over 450 deals inked in the past six years, there has been a surge in the partnership activity; majority of the collaborations have been signed for the development and manufacturing of cell therapies and antibodies.
 In order to cater the increasing demand for biologics, stake holders are actively expanding their existing capabilities; this is evident from the various acquisitions that have recently been reported.
 We expect the developers to continue to outsource their manufacturing operations in the short to mid-term, resulting in an annualized growth rate of more than 8%.
 In the long term, the projected opportunity is anticipated to be well distributed across various types of expression systems used for biomanufacturing, scale of operation and size of contract service providers

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Table of Contents

1. PREFACE
1.1. Scope of the Report
1.2. Research Methodology
1.3. Chapter Outlines

2. EXECUTIVE SUMMARY

3. INTRODUCTION
3.1. Context and Background
3.2. An Overview of Biopharmaceuticals
3.3. Biopharmaceutical Manufacturing
3.3.1. Types of Expression Systems
3.3.1.1. Bacterial Expression Systems
3.3.1.2. Yeast Expression Systems
3.3.1.3. Fungal Expression Systems
3.3.1.4. Insect Expression Systems
3.3.1.5. Plant Expression Systems
3.3.1.6. Mammalian Expression Systems

3.3.2. Manufacturing Steps
3.3.2.1. Upstream Processing
3.3.2.2. Downstream Processing

3.4. An Overview of Contract Manufacturing
3.5. Need for Outsourcing in the Biopharmaceutical Industry
3.6. Commonly Outsourced Operations in the Biopharmaceutical Industry
3.7. Basic Guidelines for Selecting a CMO Partner
3.8. Advantages of Outsourcing Manufacturing Services
3.9. Risks and Challenges Associated with Biopharmaceutical Contract Manufacturing
3.10. Concluding Remarks

4. COMPETITIVE LANDSCAPE
4.1. Chapter Overview
4.2. Biopharmaceuticals Contract Manufacturers: Overall Market Landscape
4.2.1. Analysis by Size of Employee Base
4.2.2. Analysis by Location of Headquarters
4.2.3. Analysis by Year of Establishment
4.2.4. Analysis by Location of Manufacturing Facilities
4.2.5. Analysis by Type of Biologics Manufactured
4.2.6. Analysis by Scale of Operation
4.2.7. Analysis by Expression Systems
4.2.8. Analysis by Type of Bioreactor and Modes of Operation
4.2.9. Analysis by Biomanufacturing Capacity
4.2.10. Analysis by Packaging Form
4.3. Concluding Remarks

5. BIOPHARMACEUTICAL CONTRACT MANUFACTURING IN NORTH AMERICA
5.1. Chapter Overview
5.2. Biopharmaceutical Outsourcing in the US: Regulatory Scenario
5.2.1. Impact of Current Political Situation
5.3. Leading Biopharma CMOs in North America
5.3.1. AMRI (OsoBio)
5.3.1.1. Company Overview
5.3.1.2. Services Portfolio
5.3.1.3. Financial Information
5.3.1.4. Manufacturing Facilities
5.3.1.5. Partnerships
5.3.1.6. Recent Developments
5.3.1.7. Future Outlook

5.3.2. Baxter BioPharma Solutions
5.3.2.1. Company Overview
5.3.2.2. Services Portfolio
5.3.2.3. Financial Information
5.3.2.4. Manufacturing Facilities
5.3.2.5. Partnerships
5.3.2.6. Recent Developments
5.3.2.7. Future Outlook

5.3.3. Catalent Biologics (Catalent Pharma Solutions)
5.3.3.1. Company Overview
5.3.3.2. Services Portfolio
5.3.3.3. Financial Information
5.3.3.4. Manufacturing Facilities
5.3.3.5. Partnerships
5.3.3.6. Recent Developments
5.3.3.7. Future Outlook

5.3.4. Cytovance Biologics
5.3.4.1. Company Overview
5.3.4.2. Services Portfolio
5.3.4.3. Partnerships
5.3.4.4. Recent Developments
5.3.4.5. Future Outlook

5.3.5. Patheon
5.3.5.1. Company Overview
5.3.5.2. Services Portfolio
5.3.5.3. Financial Information
5.3.5.4. Manufacturing Facilities
5.3.5.5. Partnerships
5.3.5.6. Recent Developments
5.3.5.7. Future Outlook

5.3.6. Piramal Pharma Solutions
5.3.6.1. Company Overview
5.3.6.2. Services Portfolio
5.3.6.3. Financial Information
5.3.6.4. Facilities
5.3.6.5. Partnerships
5.3.6.6. Recent Developments
5.3.6.7. Future Outlook

6. BIOPHARMACEUTICAL CONTRACT MANUFACTURING IN EUROPE
6.1. Chapter Overview
6.2. Biopharmaceutical Outsourcing in Europe: Regulatory Scenario
6.3. Leading Biopharmaceutical CMOs in Europe
6.3.1. 3P Biopharmaceuticals
6.3.1.1. Company Overview
6.3.1.2. Services Portfolio
6.3.1.3. Manufacturing Facilities
6.3.1.4. Partnerships
6.3.1.5. Recent Developments
6.3.1.6. Future Outlook

6.3.2. Boehringer Ingelheim BioXcellence™
6.3.2.1. Company Overview
6.3.2.2. Services Portfolio
6.3.2.3. Financial Information
6.3.2.4. Manufacturing Facilities
6.3.2.5. Partnerships
6.3.2.6. Recent Developments
6.3.2.7. Future Outlook

6.3.3. Celonic
6.3.3.1. Company Overview
6.3.3.2. Services Portfolio
6.3.3.3. Manufacturing Facilities
6.3.3.4. Partnerships
6.3.3.5. Recent Developments
6.3.3.6. Future Outlook

6.3.4. FUJIFILM Diosynth Biotechnologies
6.3.4.1. Company Overview
6.3.4.2. Services Portfolio
6.3.4.3. Financial Information
6.3.4.4. Manufacturing Capabilities
6.3.4.5. Partnerships
6.3.4.6. Recent Developments
6.3.4.7. Future Outlook

6.3.5. LFB Group
6.3.5.1. Company Overview
6.3.5.2. Services Portfolio
6.3.5.3. Financial Information
6.3.5.4. Manufacturing Facilities
6.3.5.5. Partnerships
6.3.5.6. Recent Developments
6.3.5.7. Future Outlook

6.3.6. Lonza
6.3.6.1. Company Overview
6.3.6.2. Services Portfolio
6.3.6.3. Financial Information
6.3.6.4. Manufacturing Facilities
6.3.6.5. Partnerships
6.3.6.6. Recent Developments
6.3.6.7. Future Outlook

6.3.7. Menarini Biotech
6.3.7.1. Company Overview
6.3.7.2. Services Portfolio
6.3.7.3. Partnerships
6.3.7.4. Future Outlook

6.3.8. Novasep
6.3.8.1. Company Overview
6.3.8.2. Services Portfolio
6.3.8.3. Financial Information
6.3.8.4. Partnerships
6.3.8.5. Recent Developments
6.3.8.6. Future Outlook

6.3.9. Rentschler BioPharma
6.3.9.1. Company Overview
6.3.9.2. Services Portfolio
6.3.9.3. Manufacturing Facilities
6.3.9.4. Partnerships
6.3.9.5. Recent Developments
6.3.9.6. Future Outlook

7. BIOPHARMACEUTICAL CONTRACT MANUFACTURING IN ASIA PACIFIC AND THE REST OF THE WORLD
7.1. Chapter Overview

7.2. Biopharmaceutical Contract Manufacturing in China
7.2.1. Biopharmaceutical Outsourcing in China: Regulatory Scenario
7.2.2. Challenges Faced while Outsourcing to China

7.3. Biopharmaceutical CMOs in China
7.3.1. AutekBio
7.3.1.1. Company Overview
7.3.1.2. Services Portfolio
7.3.1.3. Manufacturing Facilities
7.3.1.4. Future Outlook

7.3.2. WuXi AppTec (WuXi Biologics)
7.3.2.1. Company Overview
7.3.2.2. Services Portfolio
7.3.2.3. Financial Information
7.3.2.4. Manufacturing Facilities
7.3.2.5. Partnerships
7.3.2.6. Recent Developments
7.3.2.7. Future Outlook

7.4. Biopharmaceutical Contract Manufacturing in India
7.4.1. Biopharmaceutical Outsourcing in India: Regulatory Scenario
7.4.2. Challenges Faced while Outsourcing to India

7.5. Biopharmaceutical CMOs in India
7.5.1. Intas Pharmaceuticals
7.5.1.1. Company Overview
7.5.1.2. Services Portfolio
7.5.1.3. Financial Information
7.5.1.4. Manufacturing Facilities
7.5.1.5. Future Outlook

7.5.2. Kemwell Biopharma
7.5.2.1. Company Overview
7.5.2.2. Services Portfolio
7.5.2.3. Manufacturing Facilities
7.5.2.4. Partnerships
7.5.2.5. Recent Developments
7.5.2.6. Future Outlook

7.5.3. Shasun Pharmaceuticals
7.5.3.1. Company Overview
7.5.3.2. Services Portfolio
7.5.3.3. Financial Information
7.5.3.4. Future Outlook

7.5.5. Syngene
7.5.5.1. Company Overview
7.5.5.2. Services Portfolio
7.5.5.3. Financial Information
7.5.5.4. Manufacturing Facilities
7.5.5.5. Partnerships
7.5.5.6. Recent Developments
7.5.5.7. Future Outlook

7.6. Biopharmaceutical Contract Manufacturing in Japan
7.6.1. Biopharmaceutical Outsourcing in Japan: Regulatory Scenario

7.6. Biopharmaceutical CMOs in Japan
7.6.1. Asahi Glass
7.6.1.1. Company Overview
7.6.1.2. Services Portfolio
7.6.1.3. Financial Information
7.6.1.4. Manufacturing Facilities
7.6.1.5. Partnerships
7.7.1.6. Recent Developments
7.7.1.7. Future Outlook

7.7. Biopharmaceutical Contract Manufacturing in South Korea
7.7.1. Biopharmaceutical Outsourcing in South Korea: Regulatory Scenario

7.7. Biopharmaceutical CMOs in South Korea
7.7.1. DM Bio
7.7.1.1. Company Overview
7.7.1.2. Services Portfolio
7.7.1.3. Manufacturing Facilities
7.7.1.4. Future Outlook

7.7.2. Samsung BioLogics
7.7.2.1. Company Overview
7.7.2.2. Services Portfolio
7.7.2.3. Financial Information
7.7.2.4. Manufacturing Facilities
7.7.2.5. Partnerships
7.7.2.6. Recent Developments
7.7.2.7. Future Outlook

7.8. Biopharmaceutical Contract Manufacturing in Australia
7.8.1. Biopharmaceutical Outsourcing in Australia: Regulatory Scenario

7.8. Biopharmaceutical CMOs in Australia
7.8.2. Cell Therapies
7.8.2.1. Company Overview
7.8.2.2. Services Portfolio
7.8.2.3. Manufacturing Facilities
7.8.2.4. Partnerships
7.8.2.5. Recent Developments
7.8.2.6. Future Outlook

7.8.3. Luina Bio
7.8.3.1. Company Overview
7.8.3.2. Services Portfolio
7.8.3.3. Manufacturing Facilities
7.8.3.4. Partnerships
7.8.3.5. Future Outlook

8. NICHE BIOPHARMACEUTICAL SECTORS
8.1. Chapter Overview
8.2. Antibody Drug Conjugates
8.2.1. Introduction
8.2.1.1. Manufacturing Process
8.2.1.2. Key Technologies and Technology Providers

8.2.2. Pipeline Analysis
8.2.2.1. ADC Pipeline: Marketed and Clinical Molecules
8.2.2.2. ADC Pipeline: Preclinical and Discovery Stage Molecules
8.2.2.3. ADC Manufacturing: Key Challenges

8.3. Bispecific Antibodies
8.3.1. Introduction
8.3.1.1. The Bispecific Advantage
8.3.2. Pipeline Analysis
8.3.3. Bispecific Antibody Technology Providers
8.3.4. Contract Manufacturing Scenario

8.4. Cell Therapies
8.4.1. Introduction
8.4.2. Current Market Landscape
8.4.3. Cell Therapy Manufacturing
8.4.4. Cell Therapy Manufacturing Models
8.4.4.1. Centralized Manufacturing Model
8.4.4.2. Decentralized Manufacturing Model

8.4.5. Cell Therapy Manufacturing: Key Challenges and Growth Drivers
8.4.6. Important Factors for Cell Therapy Manufacturing
8.4.6.1. Cell Characterization
8.4.6.2. Cost of Goods
8.4.7. Contract Manufacturing Scenario
8.4.7.1. Analysis by Type of Cells Manufactured
8.4.7.2. Analysis by Scale of Operation

8.5. Gene Therapy
8.5.1. Introduction
8.5.2. Gene Therapy: Pipeline Analysis
8.5.2.1. Analysis by Phase of Development
8.5.2.2. Analysis by Type of Vector
8.5.2.3. Analysis by Therapeutic Area

8.5.3. Contract Manufacturing Market Landscape
8.5.3.1. Analysis by Location
8.5.3.2. Analysis by Type of Viral Vector
8.5.3.3. Analysis by Scale of Production

8.6. Plasmid DNA
8.6.1. Introduction
8.6.2. Contract Manufacturing Market Landscape
8.6.3. Analysis by Location of Manufacturing Facility
8.6.4. Analysis by Scale of Production

9. CASE STUDY: OUTSOURCING OF BIOSIMILARS
9.1. Chapter Overview
9.2. Biosimilars: An Introduction
9.3. Biosimilars: Development Stages
9.4. Regulatory Requirements for Licensing of Biosimilars
9.5. Need for Outsourcing Biosimilar Development and Manufacturing
9.6. Impact of Biosimilars on the Global Contract Manufacturing Market
9.6.1. Region-wise Distribution of Biosimilar Development / Manufacturing Activity
9.7. List of Biosimilars Contract Manufacturing Service Provider
9.8. Challenges Associated with Biosimilar Outsourcing

10. CASE STUDY: COMPARISON OF SMALL AND LARGE MOLECULE DRUGS / THERAPIES
10.1. Chapter Overview
10.2. Small Molecule and Large Molecule Drugs / Therapies
10.2.1. Comparison of General Characteristics
10.2.2. Comparison of Key Specifications
10.2.3. Comparison of Manufacturing Processes
10.2.4. Comparison of Key Manufacturing Challenges

11. CASE STUDY ON IN-HOUSE MANUFACTURING
11.1. Chapter Overview
11.2. In-House Manufacturing
11.2.1. Benefits Associated with In-House Manufacturing
11.2.2. Risks Associated with In-House Manufacturing

11.3. Outsourcing in the Biomanufacturing Industry
11.3.1. Types of Outsourcing Partners

11.4. Manufacturing Approaches Used for Approved Biologics (2016-2018)
11.4.1. Approved Biologics: Distribution by Size of Type of Manufacturing Approach
11.4.2. Approved Biologics: Distribution by Size of Developer and Type of Biologic

11.5. Choosing the Right Strategy: In-House Manufacturing versus Outsourcing

12. COLLABORATIONS
12.1. Chapter Overview
12.2. Partnership Models
12.3. Biopharmaceutical Contract Manufacturing: List of Partnerships and Collaborations
12.3.1. Analysis by Year of Partnerships
12.3.2. Analysis by Type of Partnerships
12.3.2.1. Year-Wise Trend of Product-based Agreements
12.3.2.2. Year-Wise Trend of Process-based Agreements
12.3.2.3. Year-Wise Trend of Licensing Agreements
12.3.2.4. Year-Wise Trend of Co-service Agreements / Ventures
12.3.2.5. Year-Wise Trend of R&D Agreements
12.3.2.6. Year-Wise Trend of Out-sourcing Services Agreements

12.3.3. Analysis by Focus Area
12.3.4. Analysis by Type of Biologics
12.3.4.1. Analysis by Type of Biologic and Type of Partnership Model
12.3.4.2. Analysis of Cell Therapy-related Deals by Year and Type of Partnership Model
12.3.4.3. Analysis of Monoclonal Antibody-related Deals by Year and Type of Partnership Model
12.3.4.4. Analysis of Vaccine-related Deals by Year and Type of Partnership Model
12.3.4.5. Analysis of Protein-related Deals by Year and Type of Partnership Model
12.3.4.6. Analysis of Antibody Drug Deals by Year and Type of Partnership Model
12.3.4.7. Analysis of Vector-related Deals by Year and Type of Partnership Model
12.3.4.8. Analysis of Gene Therapy-related Deals by Year and Type of Partnership Model
12.3.4.9. Analysis of Biosimilar-related Deals by Year and Type of Partnership Model
12.3.4.10. Analysis of Other Biologic-related Deals by Type of Partnership Model
12.3.4.11. Analysis by Type of Biologics and Geography

12.3.5. Analysis by Therapeutic Area
12.3.6. Analysis of Most Active Players by Number of Partnerships
12.3.7. Regional Analysis
12.3.7.1. Intercontinental and Intracontinental Agreements

12.4. Mergers and Acquisitions
12.4.1. Acquisitions Models
12.4.2. Biopharmaceutical Contract Manufacturing: Mergers and Acquisitions
12.4.3. Cumulative Year-wise Trend
12.4.4. Analysis by Type of Acquisition
12.4.5. Geographical Activity
12.4.5.1. Mergers and Acquisitions: Continent-wise Distribution
12.4.5.2. Mergers and Acquisitions: Country-wise Distribution
12.4.5.3. Mergers and Acquisitions: Intercontinental and Intracontinental Deals

12.4.6. Most Active Acquirers: Analysis by Number of Acquisitions
12.4.7 Mergers and Acquisitions: Distribution by Key Value Drivers and Type of Biologics
12.4.7.1. Mergers and Acquisitions: Analysis by Key Value Drivers
12.4.7.2. Mergers and Acquisitions: Analysis by Key Value Drivers and Year of Acquisition
12.4.7.3. Mergers and Acquisitions: Analysis by Type of Biologics
12.4.7.4. Mergers and Acquisitions: Analysis by Type of Biologics and Key Value Drivers
12.5. Key Acquisitions: Deal Multiples

13. RECENT DEVELOPMENTS
13.1. Chapter Overview
13.2. Biopharma Contract Manufacturing Market: Facility Expansions
13.2.1. Cumulative Year-wise Distribution
13.2.2. Analysis by Purpose of Facility Expansion
13.2.3. Analysis by Type of Biologics
13.2.4. Analysis by Type of Biologics and Purpose of Expansion
13.2.5. Analysis by Location of Manufacturing Facility
13.2.6. Regional Analysis
13.2.7. Most Active Players: Analysis by Number of Recent Expansions
13.2.8. Analysis by Headquarters and Purpose
13.2.9. Facility Expansions: Pre-2015 and Post-2015
13.3. Biopharmaceutical Contract Manufacturing Market: Funding Instances
13.4. Technological Advancements
13.4.1. Single Use Technology
13.4.2. Process Analytical Technology (PAT)
13.4.3. Continuous Processing
13.4.3. Quality by Design in Bioprocessing


13.3. Biopharmaceutical Contract Manufacturing Market: Funding Instances
13.4. Technological Advancements
13.4.1. Single Use Technology
13.4.2. Process Analytical Technology
13.4.3. Continuous Processing
13.4.4. Quality by Design in Bioprocessing

14. CAPACITY ANALYSIS
14.1. Chapter Overview
14.2. Assumptions and Methodology
14.3. Biopharmaceutical Contract Manufacturers: Global Production Capacity
14.3.1. Analysis by Size of the CMO
14.3.2. Analysis by Expression Systems
14.3.3. Analysis by Scale of Operation
14.3.4. Analysis by Region
14.3.4.1. Capacity Analysis: North America
14.3.4.2. Capacity Analysis: Europe
14.3.4.3. Capacity Analysis: Asia and Middle East
14.4. Emerging Biologics: Capacity Analysis
14.4.1. ADC Manufacturing Installed Global Capacity: Regional Distribution
14.5. Cell Therapy Manufacturing Capacity: Regional Distribution
14.6. Viral Vectors Installed Manufacturer Capacity: Distribution by Location of Manufacturing Facility
14.7. Concluding Remarks

15. DEMAND ANALYSIS
15.1. Chapter Overview
15.2. Key Assumptions and Methodology
15.3. Overall Annual Demand for Biopharmaceutical Market, 2019-2024
15.3.1. Analysis by Therapeutic Area

15.4. Relationship Between Annual Demand and Capacity
15.5. Demand for Emerging Novel Biologics
15.5.1. ADCs: Overall Annual Demand
15.5.1. ADCs: Demand and Supply Analysis

16. MARKET FORECAST
16.1. Chapter Overview
16.2. Forecast Methodology and Key Assumptions

16.3. Overall Biopharmaceutical Contract Manufacturing Market, 2019-2030
16.3.1. Biopharmaceutical Contract Manufacturing Market for API Manufacturing, 2019-2030
16.3.2. Biopharmaceutical Contract Manufacturing Market for FDF Manufacturing, 2019-2030

16.4. Biopharmaceutical Contract Manufacturing Market, 2019-2030: Distribution by Expression Systems Used
16.5. Biopharmaceutical Contract Manufacturing Market, 2019-2030: Distribution by Scale of Operation
16.6. Biopharmaceutical Contract Manufacturing Market, 2019-2030: Distribution by Size of Manufacturers

16.7. Biopharmaceutical Contract Manufacturing Market, 2019-2030: Distribution by Geography
16.7.1. Biopharmaceutical Contract Manufacturing Market in North America, 2019-2030
16.7.1.1. Biopharmaceutical Contract Manufacturing Market in the US, 2019-2030
16.7.1.2. Biopharmaceutical Contract Manufacturing Market in Canada, 2019-2030
16.7.1.3. Biopharmaceutical Contract Manufacturing Market in North America, 2019-2030: Share of Mammalian Cell-based Operations
16.7.1.4. Biopharmaceutical Contract Manufacturing Market in North America, 2019-2030: Share of Microbial Cell-based Operations
16.7.1.5. Biopharmaceutical Contract Manufacturing Market in North America, 2019-2030: Share of Other Expression System-based Operations
16.7.1.6. Biopharmaceutical Contract Manufacturing Market in North America, 2019-2030: Share of Preclinical / Clinical Scale Operations
16.7.1.7. Biopharmaceutical Contract Manufacturing Market in North America, 2019-2030: Share of Commercial Scale Operations
16.7.1.8. Biopharmaceutical Contract Manufacturing Market in North America, 2019-2030: Share of Small-sized Companies
16.7.1.9. Biopharmaceutical Contract Manufacturing Market in North America, 2019-2030: Share of Mid-sized Companies
16.7.1.10. Biopharmaceutical Contract Manufacturing Market in North America, 2019-2030: Share of Large / Very Large Companies

16.7.2. Biopharmaceutical Contract Manufacturing Market in Europe, 2019-2030
16.7.2.1. Biopharmaceutical Contract Manufacturing Market in Italy, 2019-2030
16.7.2.2. Biopharmaceutical Contract Manufacturing Market in Germany, 2019-2030
16.7.2.3. Biopharmaceutical Contract Manufacturing Market in France, 2019-2030
16.7.2.4. Biopharmaceutical Contract Manufacturing Market in Spain, 2019-2030
16.7.2.5. Biopharmaceutical Contract Manufacturing Market in the UK, 2019-2030
16.7.2.6. Biopharmaceutical Contract Manufacturing Market in Rest of Europe, 2019-2030

16.7.2.7. Biopharmaceutical Contract Manufacturing Market in Europe, 2019-2030: Share of Mammalian Cell-based Operations
16.7.2.8. Biopharmaceutical Contract Manufacturing Market in Europe, 2019-2030: Share of Microbial Cell-based Operations
16.7.2.9. Biopharmaceutical Contract Manufacturing Market in Europe, 2019-2030: Share of Other Expression System-based Operations

16.7.2.10. Biopharmaceutical Contract Manufacturing Market in Europe, 2019-2030: Share of Preclinical / Clinical Operations
16.7.2.11. Biopharmaceutical Contract Manufacturing Market in Europe, 2019-2030: Share of Commercial Operations
16.7.2.12. Biopharmaceutical Contract Manufacturing Market in Europe, 2019-2030: Share of Small-sized Companies
16.7.2.13. Biopharmaceutical Contract Manufacturing Market in Europe, 2019-2030: Share of Mid-sized Companies
16.7.2.14. Biopharmaceutical Contract Manufacturing Market in Europe, 2019-2030: Share of Large / Very Large Companies

16.7.3. Biopharmaceutical Contract Manufacturing Market in Asia and Rest of the World, 2019-2030
16.7.3.1. Biopharmaceutical Contract Manufacturing Market in China, 2019-2030
16.7.3.2. Biopharmaceutical Contract Manufacturing Market in India, 2019-2030
16.7.3.3. Biopharmaceutical Contract Manufacturing Market in South Korea, 2019-2030
16.7.3.4. Biopharmaceutical Contract Manufacturing Market in Japan, 2019-2030
16.7.3.5. Biopharmaceutical Contract Manufacturing Market in Australia, 2019-2030
16.7.3.6. Biopharmaceutical Contract Manufacturing Market in Rest of Asia and Other Regions, 2019-2030

16.7.3.7. Biopharmaceutical Contract Manufacturing Market in Asia and Rest of the World, 2019-2030: Share of Mammalian Cell-based Operations
16.7.3.8. Biopharmaceutical Contract Manufacturing Market in Asia and Rest of the World, 2019-2030: Share of Microbial Cell-based Operations
16.7.3.9. Biopharmaceutical Contract Manufacturing Market in Asia and Rest of the World, 2019-2030: Share of Other Expression System-based Operations

16.7.3.10. Biopharmaceutical Contract Manufacturing Market in Asia and Rest of the World, 2019-2030: Share of Preclinical / Clinical Operations
16.7.3.11. Biopharmaceutical Contract Manufacturing Market in Asia and Rest of the World, 2019-2030: Share of Commercial Scale Operations

16.7.3.12. Biopharmaceutical Contract Manufacturing Market in Asia and Rest of the World, 2019-2030: Share of Small-sized Companies
16.7.3.13. Biopharmaceutical Contract Manufacturing Market in Asia and Rest of the World, 2019-2030: Share of Mid-sized Companies
16.7.3.14. Biopharmaceutical Contract Manufacturing Market in Asia and Rest of the World, 2019-2030: Large / Very Large Companies
16.7.4 Overall Biopharmaceutical Contract Manufacturing, 2019-2030: Share by Others Segment

17. SWOT ANALYSIS
17.1 Chapter Overview
17.2. Strengths
17.3. Weaknesses
17.4. Opportunities
17.5. Threats
17.6. Comparison of Swot Factors
17.7. Concluding Remarks

18. FUTURE OF THE BIOPHARMACEUTICAL CMO MARKET
18.1. Chapter Overview
18.2. Outsourcing Activities to Witness Significant Growth in the Coming Years
18.3. Shift from One-time Contracts to Strategic Partnerships
18.4. Integration / Adoption of New and Innovative Technologies
18.4.1. Single use Bioreactors
18.4.2. Novel Bioprocess Techniques
18.4.3. Bioprocess Automation

18.5. Focus on Niche Therapeutic Areas
18.6. Growing Biosimilars Market to Contribute to the Growth of the Contract Services Segment
18.7. Capability and Expertise Expansions by CMOs to become One Stop Shops
18.8. Offshoring Outsourcing Activities to Maximize Profits and Expand Existing Capacities
18.9. Increase in Financial Inflow and Outsourcing Budgets
18.10. The Need for Humanized Products to Drive the Growth of Mammalian Expression Technologies

18.11. Challenges Faced by both Sponsors and Service Providers
18.11.1. Concerns related to Single Use Systems
18.11.2. Issues Related to Capacity Fluctuations

18.12. Concluding Remarks

19. SURVEY ANALYSIS
19.1. Chapter Overview
19.1.1. Overview of Respondents
19.1.2. Designation of Respondents

19.2. Biologics Manufacturing Expertise
19.3. Scale of Manufacturing
19.4. Location of Production Facilities
19.5. Types of Expression Systems Used
19.6. Types of Bioreactors
19.7. Modes of Operation of Bioreactors

20. INTERVIEW TRANSCRIPTS
20.1. Chapter Overview
20.2. Astrid Brammer, Senior Manager Business Development, Richter-Helm
20.3. Birgit Schwab, Senior Manager Strategic Marketing, Rentschler Biotechnologie
20.4. Christian Bailly, Director of CDMO, Pierre Fabre
20.5. Claire Otjes, Assistant Marketing Manager, Batavia Biosciences
20.6. David C Cunningham, Director Corporate Development, Goodwin Biotechnology
20.7. Dietmar Katinger, Chief Executive Officer, Polymun Scientific
20.8. Denis Angioletti, Chief Commercial Officer, Cerbios-Pharma
20.9. Jeffrey Hung, Chief Commercial Officer, Vigene Biosciences
20.10. Kevin Daley, Director Pharmaceuticals, Novasep
20.11. Mark Wright, Site Head, Grangemouth, Piramal Healthcare
20.12. Nicolas Grandchamp, R&D Leader, GEG Tech
20.13. Raquel Fortunato, Chief Executive Officer, GenIbet Biopharmaceuticals
20.14. Sebastian Schuck, Head of Business Development, Wacker Biotech
20.15. Stephen Taylor, Senior Vice President Commercial, FUJIFILM Diosynth Biotechnologies
20.16. Tatjana Buchholz, Marketing Manager, PlasmidFactory and Marco Schmeer, Project Manager, Plasmid Factory
20.17. Tim Oldham, Chief Executive Officer, Cell Therapies

21. APPENDIX 1: LIST OF NON-INDUSTRY PLAYERS

22. APPENDIX 2: TABULATED DATA

23. APPENDIX 3: LIST OF COMPANIES AND ORGANIZATIONS


Contact Details

Gaurav Chaudhary
+1 (415) 800 3415
[email protected]