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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and 250+ tables, please visit this https://www.rootsanalysis.com/reports/250/request-sample.html
Key Market Insights
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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
