Roots Analysis has done a detailed study on “Medical Device CRO
Market (2nd Edition), 2020-2030”. covering various important aspects of the industry and
identifying key future growth opportunities.
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and 200+ tables, please visit this - https://www.rootsanalysis.com/reports/view_document/medical-device-cros-market/226.html
Key Market Insights
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For more information, please visit https://www.rootsanalysis.com/reports/view_document/medical-device-cros-market/226.html
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. Chapter Overview
3.2. Overview of Medical Devices
3.2.1. Historical Evolution of Medical
Devices
3.2.2. Classification of Medical
Devices
3.3. Overview of Contract Research Organizations (CROs)
3.3.1. Evolution of CROs
3.4. Role of CROs in the Medical Device Industry
3.5. Types of Medical Device CROs
3.6. Types of Services Offered by CROs
3.7. Advantages of Outsourcing Operations to CROs
3.8. Risks and Challenges Associated with Outsourcing
3.9. Key Considerations for Selecting a Suitable CRO
Partner
4. MARKET LANDSCAPE
4.1. Chapter
Overview
4.2. Medical Device CROs: Clinical Service Providers
4.2.1. Analysis
by Year of Establishment
4.2.2. Analysis
by Company Size
4.2.3. Analysis
by Location of Headquarters
4.2.4. Analysis
by Company Size and Location of Headquarters
4.2.5. Analysis by Area of
Specialization
4.2.6. Analysis
by Device Class
4.2.7. Analysis
by Type of Clinical Operation Services Offered
4.2.8. Analysis by Type of Regulatory
Affairs-related Services Offered
4.2.9. Analysis by Type of Additional
Services Offered
4.2.10. Analysis by Medical Device
Regulatory Compliance Authorities
4.3. Medical Device CROs: Preclinical Service Providers
4.3.1. Analysis
by Year of Establishment
4.3.2. Analysis
by Company Size
4.3.3. Analysis
by Location of Headquarters
4.3.4. Analysis
by Company Size and Location of Headquarters
4.3.5. Analysis
by Type of Preclinical Services Offered
4.4. Medical Device CROs: Standalone Service Providers
4.4.1. Analysis
by Year of Establishment
4.4.2. Analysis
by Company Size
4.4.3. Analysis
by Location of Headquarters
4.4.4. Analysis
by Company Size and Location of Headquarters
5. REGULATORY
AND REIMBURSEMENT LANDSCAPE FOR MEDICAL DEVICES
5.1. Chapter Overview
5.2. General Regulatory and Reimbursement Guidelines
for Medical Devices
5.3. Regulatory and Reimbursement Landscape in North
America
5.3.1. The US Scenario
5.3.1.1. Regulatory
Authority
5.3.1.2. Review
/ Approval Process
5.3.1.3. Reimbursement
Landscape
5.3.1.3.1. Payer Mix
5.3.1.3.2. Reimbursement Process
5.3.2. The Canadian Scenario
5.3.2.1. Regulatory
Authority
5.3.2.2. Review
/ Approval Process
5.3.2.3. Reimbursement
Landscape
5.3.2.3.1. Payer Mix
5.3.2.3.2. Reimbursement Process
5.3.3. The Mexican Scenario
5.3.3.1. Regulatory
Authority
5.3.3.2. Review
/ Approval Process
5.3.3.3. Reimbursement
Landscape
5.3.3.3.1. Payer Mix
5.4. Regulatory and Reimbursement Landscape in Europe
5.4.1. Overall Scenario
5.4.1.1. Overall
Regulatory Authority
5.4.1.2. Overall
Review / Approval Process
5.4.2. The UK Scenario
5.4.2.1. Regulatory
Authority
5.4.2.2. Review
/ Approval Process
5.4.2.3. Reimbursement
Landscape
5.4.2.3.1. Payer Mix
5.4.2.3.2. Reimbursement Process
5.4.3. The French Scenario
5.4.3.1. Regulatory
Authority
5.4.3.2. Review
/ Approval Process
5.4.3.3. Reimbursement
Landscape
5.4.3.3.1. Payer Mix
5.4.3.3.2. Reimbursement Process
5.4.4. The German Scenario
5.4.4.1. Regulatory
Authority
5.4.4.2. Review
/ Approval Process
5.4.4.3. Reimbursement
Landscape
5.4.4.3.1. Payer Mix
5.4.4.3.2. Reimbursement Process
5.4.5. The Italian Scenario
5.4.5.1. Regulatory
Authority
5.4.5.2. Review
/ Approval Process
5.4.5.3. Reimbursement
Landscape
5.4.5.3.1. Payer Mix
5.4.5.3.2. Reimbursement Process
5.4.6. The Spanish Scenario
5.4.6.1. Regulatory
Authority
5.4.6.2. Review
/ Approval Process
5.4.6.3. Reimbursement
Landscape
5.4.6.3.1. Payer Mix
5.4.6.3.2. Reimbursement Process
5.5. Regulatory and Reimbursement Landscape in
Asia-Pacific and Rest of the World
5.5.1. The Australian Scenario
5.5.1.1. Regulatory
Authority
5.5.1.2. Review
/ Approval Process
5.5.1.3. Reimbursement
Landscape
5.5.1.3.1. Payer Mix
5.5.1.3.2. Reimbursement Process
5.5.2. The Brazilian Scenario
5.5.2.1. Regulatory
Authority
5.5.2.2. Review
/ Approval Process
5.5.2.3. Reimbursement
Landscape
5.5.2.3.1. Payer Mix
5.5.2.3.2. Reimbursement Process
5.5.3. The Chinese Scenario
5.5.3.1. Regulatory
Authority
5.5.3.2. Review
/ Approval Process
5.5.3.3. Reimbursement
Landscape
5.5.3.3.1. Payer Mix
5.5.3.3.2. Reimbursement Process
5.5.4. The Indian Scenario
5.5.4.1. Regulatory
Authority
5.5.4.2. Review
/ Approval Process
5.5.4.3. Reimbursement
Landscape
5.5.4.3.1. Payer Mix
5.5.5. The Israeli Scenario
5.5.5.1. Regulatory
Authority
5.5.5.2. Review
/ Approval Process
5.5.5.3. Reimbursement
Landscape
5.5.5.3.1. Payer Mix
5.5.6. The Japanese Scenario
5.5.6.1. Regulatory
Authority
5.5.6.2. Review
/ Approval Process
5.5.6.3. Reimbursement
Landscape
5.5.6.3.1. Payer Mix
5.5.6.3.2. Reimbursement Process
5.5.7. The New Zealand Scenario
5.5.7.1. Regulatory
Authority
5.5.7.2. Review
/ Approval Process
5.5.7.3. Reimbursement
Landscape
5.5.7.3.1. Payer Mix
5.5.7.3.2. Reimbursement Process
5.5.8. The Singapore Scenario
5.5.8.1. Regulatory
Authority
5.5.8.2. Review
/ Approval Process
5.5.8.3. Reimbursement
Landscape
5.5.8.3.1. Payer Mix
5.5.8.3.2. Reimbursement Process
5.5.9. The South Korean Scenario
5.5.9.1. Regulatory
Authority
5.5.9.2. Review
/ Approval Process
5.5.9.3. Reimbursement
Landscape
5.5.9.3.1. Payer Mix
5.5.9.3.2. Reimbursement Process
5.5.10. The South African Scenario
5.5.10.1. Regulatory Authority
5.5.10.2. Review / Approval Process
5.5.10.3. Reimbursement Landscape
5.5.11. The Taiwan Scenario
5.5.11.1. Regulatory Authority
5.5.11.2. Review / Approval Process
5.5.11.3. Reimbursement Landscape
5.5.11.3.1. Payer Mix
5.5.11.3.2. Reimbursement Process
5.5.12. The Thailand Scenario
5.5.12.1. Regulatory Authority
5.5.12.2. Review / Approval Process
5.5.12.3. Reimbursement Landscape
5.6. Comparison of Regional Regulatory Control
5.7. Concluding Remarks
6. COMPANY
PROFILES
6.1. Chapter Overview
6.2. Avania (Formerly known as Factory CRO)
6.2.1. Company Overview
6.2.2. Service Portfolio
6.2.3. Future Outlook
6.3. Charles River Laboratories
6.3.1. Company Overview
6.3.2. Service Portfolio
6.3.3. Future Outlook
6.4. Clinlogix
6.4.1. Company Overview
6.4.2. Service Portfolio
6.4.3. Future Outlook
6.5. CROMSOURCE
6.5.1. Company Overview
6.5.2. Service Portfolio
6.5.3. Future Outlook
6.6. CSSi LifeSciences
6.6.1. Company Overview
6.6.2. Service Portfolio
6.6.3. Future Outlook
6.7. Eurofins Medical device Testing
6.7.1. Company Overview
6.7.2. Service Portfolio
6.7.3. Future Outlook
6.8. genae
6.8.1. Company Overview
6.8.2. Service Portfolio
6.8.3. Future Outlook
6.9. IMARC Research
6.9.1. Company Overview
6.9.2. Service Portfolio
6.9.3. Future Outlook
6.10. IQVIA
6.10.1. Company Overview
6.10.2. Service Portfolio
6.10.3. Future Outlook
6.11. Medpace
6.11.1. Company Overview
6.11.2. Service Portfolio
6.11.3. Future Outlook
6.12. NAMSA
6.12.1. Company Overview
6.12.2. Service Portfolio
6.12.3. Future Outlook
6.13. Qserve Group
6.13.1. Company Overview
6.13.2. Service Portfolio
6.13.3. Future Outlook
6.14. Regulatory and Clinical Research Institute (Now a
part of Covance)
6.14.1. Company Overview
6.14.2. Service Portfolio
6.14.3. Future Outlook
6.15. WuXi AppTec
6.15.1. Company Overview
6.15.2. Service Portfolio
6.15.3. Future Outlook
7. MEDICAL
DEVICE DEVELOPER AND CRO RELATIONSHIPS: KEY VALUE DRIVERS AND PERFORMANCE INDICATORS
7.1. Chapter Overview
7.2. Definition and Importance of Key Performance
Indicators (KPIs)
7.3. Key Considerations for Selection of KPIs
7.4. Types of KPIs
7.4.1. Financial Indicators
7.4.1.1. Most Important KPIs
7.4.1.1.1. Financial Stability
7.4.1.1.2. Cost of Services Offered
7.4.1.1.3. Comparative Analysis of Financial
Indicators
7.4.1.2. Industry Perspective
7.4.1.2.1. Sponsors’ (Big Pharma) Perspective
7.4.1.2.2. Contract Service Providers’ Perspective
7.4.2. Process and Capability Indicators
7.4.2.1. Most Important KPIs
7.4.2.1.1. Proximity to Sponsor
7.4.2.1.2. Capability to Innovate / Mitigate Risk
7.4.2.1.3. Strength of Service Portfolio
7.4.2.1.4. Comparative Analysis of Process /
Capability Indicators
7.4.2.2. Industry Perspective
7.4.2.2.1. Sponsors’ (Big Pharma) Perspective
7.4.2.2.2. Contract Service Providers’ Perspective
7.4.3. Market Reputation Indicators
7.4.3.1. Most Important KPIs
7.4.3.1.1. Flexibility / Adaptability
7.4.3.1.2. Time Management
7.4.3.1.3. Quality / Reliability
7.4.3.1.4. Regulatory Compliance / Track Record
7.4.3.1.5. Comparative Analysis of Market
Reputation Indicators
7.4.3.2. Industry Perspective
7.4.3.2.1. Sponsors’ (Big Pharma) Perspective
7.4.3.2.2. Contract Service Providers’ Perspective
7.5. Comparison of Key Performance Indicators
7.6. Concluding Remarks
8. COMPETITIVE
BENCHMARKING
8.1. Chapter Overview
8.2. Assumptions and Methodology
8.3. Competitive Benchmarking by Region
8.3.1. North America, Peer Group I
8.3.2. North America, Peer Group II
8.3.3. North America, Peer Group III
8.3.4. Europe, Peer Group IV
8.3.5. Europe, Peer Group V
8.3.6. Europe, Peer Group VI
8.3.7. Asia-Pacific, Peer Group VII
8.3.8. Asia-Pacific, Peer Group VIII
8.3.9. RoW, Peer Group IX
8.4. Concluding Remarks
9. BRAND
POSITIONING OF KEY INDUSTRY PLAYERS
9.1. Chapter Overview
9.2. Scope and Methodology
9.3. Brand Positioning Matrix: Labcorp
9.4. Brand Positioning Matrix: IQVIA
9.5. Brand Positioning Matrix: Syneos Health
9.6. Brand Positioning Matrix: PPD
9.7. Brand Positioning Matrix: ICON
9.8. Brand Positioning Matrix: Charles River
Laboratories
9.9. Brand Positioning Matrix: WuXi AppTec
9.10. Brand Positioning Matrix:
Medpace
9.11. Brand Positioning Matrix:
PAREXEL International
9.12. Brand Positioning Matrix: NAMSA
10. CLINICAL
TRIAL ANALYSIS
10.1. Chapter Overview
10.2. Scope and Methodology
10.3. Medical Devices: Clinical Trial Analysis
10.3.1. Analysis by Trial Registration
Year
10.3.2. Analysis by Trial Status
10.3.3. Analysis by Trial Phase
10.3.4. Analysis by Therapeutic Area
10.3.5. Analysis by Geography
10.3.6. Geographical Analysis by Trial
Status
10.4. Analysis by Type of Sponsor
10.5. Medical Devices: Analysis of Enrolled Patient
Population
10.5.1. Analysis by Trial Registration
Year
10.5.2. Analysis by Trial Status
10.5.3. Analysis by Trial Phase
10.5.4. Analysis by Therapeutic Area
10.5.5. Analysis by Location of Trial Site
10.5.6. Analysis by Trial Status and
Location of Trial Site
11. MERGERS
AND ACQUISITIONS
11.1. Chapter Overview
11.2. Merger and Acquisition Models
11.3. Medical Device
CROs: Mergers and Acquisitions
11.3.1. Analysis
by Year of Merger / Acquisition
11.3.2. Analysis by Type of Agreement
11.3.3. Regional
Analysis
11.3.3.1. Continent-wise Distribution
11.3.3.2. Intercontinental and Intracontinental
Deals
11.3.3.3. Country-wise Distribution
11.3.4. Ownership
Change Matrix
11.3.5. Analysis
by Type of Company
11.3.6. Analysis by Key Value Drivers
11.3.6.1. Analysis by Key Value Drivers and
Year of Acquisition
12. SURVEY
INSIGHTS
12.1. Chapter Overview
12.2. Designation of Respondents
12.3. Type of Service Offered
12.4. Target Therapeutic Area
12.5. Number of Annual Projects
12.6. Market Opportunity
13. MARKET
SIZING AND FORECAST
13.1. Chapter Overview
13.2. Assumptions and Forecast
Methodology
13.3. Overall Medical Device CRO
Market, 2020-2030
13.3.1. Medical
Device CRO Market, 2020-2030: Distribution by Therapeutic Area
13.3.2. Medical Device CRO Market,
2020-2030: Distribution by Scale of Operation
13.3.3. Medical Device CRO Market,
2020-2030: Distribution by Device Class
13.3.4. Medical
Device CRO Market, 2020-2030: Distribution by Type of Clinical Service Offered
13.3.5. Medical
Device CRO Market, 2020-2030: Distribution by Type of Preclinical Service Offered
13.3.6. Medical Device CRO Market,
2020-2030: Distribution by Geography
13.4. Medical
Device CRO Market in North America, 2020-2030
13.4.1. Medical Device CRO Market in North
America, 2020-2030: Distribution by Therapeutic Area
13.4.1.1. Medical Device CRO Market for CNS
Disorders in North America, 2020-2030
13.4.1.2. Medical Device CRO Market for
Cardiovascular Disorders in North America, 2020-2030
13.4.1.3. Medical Device CRO Market for
Oncological Disorders in North America, 2020-2030
13.4.1.4. Medical Device CRO Market for Bone
Disorders in North America, 2020-2030
13.4.1.5. Medical Device CRO Market for
Respiratory Disorders in North America, 2020-2030
13.4.1.6. Medical Device CRO Market for Pain Management Disorders in
North America, 2020- 2030
13.4.1.7. Medical Device CRO Market for Ophthalmic
Disorders in North America, 2020-2030
13.4.1.8. Medical Device CRO Market for
Psychological Disorders in North America, 2020-2030
13.4.1.9. Medical Device CRO Market for
Metabolic Disorders in North America, 2020-2030
13.4.1.10. Medical Device CRO Market for Other
Therapeutic Areas in North America, 2020-2030
13.4.2. Medical
Device CRO Market in North America, 2020-2030: Distribution by Device Class
13.4.2.1. Medical Device CRO Market for Class I
Devices in North America, 2020-2030
13.4.2.2. Medical Device CRO Market for Class II
Devices in North America, 2020-2030
13.4.2.3. Medical Device CRO Market for Class
III Devices in North America, 2020-2030
13.4.3. Medical Device CRO Market in North
America, 2020-2030: Distribution by Type of Clinical
Service Offered
13.4.3.1. Medical Device CRO Market for Clinical Trial Management
Services in North America, 2020-2030
13.4.3.2. Medical Device CRO Market for
Consulting Services in North America, 2020-2030
13.4.3.3. Medical Device CRO Market for Data Management Services in
North America, 2020-2030
13.4.3.4. Medical Device CRO Market for Regulatory Affairs Management
Services in North America, 2020-2030
13.4.3.5. Medical Device CRO Market for Other
Clinical Services in North America, 2020-2030
13.4.4. Medical Device CRO Market in North
America, 2020-2030: Distribution by Type of Preclinical
Service Offered
13.4.4.1. Medical Device CRO Market for Material Characterization and
Analytical Services in North
America, 2020-2030
13.4.4.2. Medical Device CRO Market for Biocompatibility Testing
Services in North America, 2020-2030
13.4.4.3. Medical Device CRO Market for
Sterility and Microbiology Testing Services in North America,
2020-2030
13.4.4.4. Medical Device CRO Market for Other Preclinical Services in
North America, 2020- 2030
13.5. Medical
Device CRO Market in Europe, 2020-2030
13.5.1. Medical
Device CRO Market in Europe, 2020-2030: Distribution by Therapeutic Area
13.5.1.1. Medical Device CRO Market for CNS Disorders
in Europe, 2020-2030
13.5.1.2. Medical Device CRO Market for
Cardiovascular Disorders in Europe, 2020-2030
13.5.1.3. Medical Device CRO Market for
Oncological Disorders in Europe, 2020-2030
13.5.1.4. Medical Device CRO Market for Bone
Disorders in Europe, 2020-2030
13.5.1.5. Medical Device CRO Market for
Respiratory Disorders in Europe, 2020-2030
13.5.1.6. Medical Device CRO Market for Pain
Management Disorders in Europe, 2020-2030
13.5.1.7. Medical Device CRO Market for
Ophthalmic Disorders in Europe, 2020-2030
13.5.1.8. Medical Device CRO Market for
Psychological Disorders in Europe, 2020-2030
13.5.1.9. Medical Device CRO Market for
Metabolic Disorders in Europe, 2020-2030
13.5.1.10. Medical Device CRO Market for Other
Therapeutic Areas in Europe, 2020-2030
13.5.2. Medical
Device CRO Market in Europe, 2020-2030: Distribution by Device Class
13.5.2.1. Medical Device CRO Market for Class I
Devices in Europe, 2020-2030
13.5.2.2. Medical Device CRO Market for Class II
Devices in Europe, 2020-2030
13.5.2.3. Medical Device CRO Market for Class
III Devices in Europe, 2020-2030
13.5.3. Medical Device CRO Market in Europe,
2020-2030: Distribution by Type of Clinical Service
Offered
13.5.3.1. Medical Device CRO Market for Clinical Trial Management
Services in Europe, 2020-2030
13.5.3.2. Medical Device CRO Market for
Consulting Services in Europe, 2020-2030
13.5.3.3. Medical Device CRO Market for Data
Management Services in Europe, 2020-2030
13.5.3.4. Medical Device CRO Market for Regulatory Affairs Management
Services in Europe, 2020-2030
13.5.3.5. Medical Device CRO Market for Other
Clinical Services in Europe, 2020-2030
13.5.4. Medical Device CRO Market in Europe,
2020-2030: Distribution by Type of Preclinical Service
Offered
13.5.4.1. Medical Device CRO Market for Material Characterization and
Analytical Services in Europe,
2020-2030
13.5.4.2. Medical Device CRO Market for Biocompatibility Testing
Services in Europe, 2020-2030
13.5.4.3. Medical Device CRO Market for Sterility and Microbiology
Testing Services in Europe, 2020-2030
13.5.4.4. Medical Device CRO Market for Other
Preclinical Services in Europe, 2020-2030
13.6. Medical
Device CRO Market in Asia-Pacific, 2020-2030
13.6.1. Medical Device CRO Market in
Asia-Pacific, 2020-2030: Distribution by Therapeutic Area
13.6.1.1. Medical Device CRO Market for CNS
Disorders in Asia-Pacific, 2020-2030
13.6.1.2. Medical Device CRO Market for
Cardiovascular Disorders in Asia-Pacific, 2020-2030
13.6.1.3. Medical Device CRO Market for
Oncological Disorders in Asia-Pacific, 2020-2030
13.6.1.4. Medical Device CRO Market for Bone
Disorders in Asia-Pacific, 2020-2030
13.6.1.5. Medical Device CRO Market for
Respiratory Disorders in Asia-Pacific, 2020-2030
13.6.1.6. Medical Device CRO Market for Pain Management Disorders in
Asia-Pacific, 2020-2030
13.6.1.7. Medical Device CRO Market for
Ophthalmic Disorders in Asia-Pacific, 2020-2030
13.6.1.8. Medical Device CRO Market for Psychological
Disorders in Asia-Pacific, 2020-2030
13.6.1.9. Medical Device CRO Market for
Metabolic Disorders in Asia-Pacific, 2020-2030
13.6.1.10. Medical Device CRO Market for Other
Therapeutic Areas in Asia-Pacific, 2020-2030
13.6.2. Medical
Device CRO Market in Asia-Pacific, 2020-2030: Distribution by Device Class
13.6.2.1. Medical Device CRO Market for Class I
Devices in Asia-Pacific, 2020-2030
13.6.2.2. Medical Device CRO Market for Class II
Devices in Asia-Pacific, 2020-2030
13.6.2.3. Medical Device CRO Market for Class
III Devices in Asia-Pacific, 2020-2030
13.6.3. Medical Device CRO Market in
Asia-Pacific, 2020-2030: Distribution by Type of Clinical Service Offered
13.6.3.1. Medical Device CRO Market for Clinical
Trial Management Services in Asia-Pacific, 2020-2030
13.6.3.2. Medical Device CRO Market for
Consulting Services in Asia-Pacific, 2020-2030
13.6.3.3. Medical Device CRO Market for Data
Management Services in Asia-Pacific, 2020-2030
13.6.3.4. Medical Device CRO Market for Regulatory Affairs Management
Services in Asia-Pacific, 2020-2030
13.6.3.5. Medical Device CRO Market for Other
Clinical Services in Asia-Pacific, 2020-2030
13.6.4. Medical Device CRO Market in
Asia-Pacific, 2020-2030: Distribution by Type of Preclinical Service Offered
13.6.4.1. Medical Device CRO Market for Material Characterization and
Analytical Services in Asia-Pacific,
2020-2030
13.6.4.2. Medical Device CRO Market for
Biocompatibility Testing Services in Asia-Pacific, 2020- 2030
13.6.4.3. Medical Device CRO Market for
Sterility and Microbiology Testing Services in Asia- Pacific,
2020-2030
13.6.4.4. Medical Device CRO Market for Other
Preclinical Services in Asia-Pacific, 2020-2030
13.7. Medical
Device CRO Market in Rest of the World, 2020-2030
13.7.1. Medical
Device CRO Market in Rest of the World, 2020-2030: Distribution by Therapeutic Area
13.7.1.1. Medical Device CRO Market for CNS
Disorders in Rest of the World, 2020-2030
13.7.1.2. Medical Device CRO Market for Cardiovascular Disorders in
Rest of the World, 2020-2030
13.7.1.3. Medical Device CRO Market for
Oncological Disorders in Rest of the World, 2020-2030
13.7.1.4. Medical Device CRO Market for Bone
Disorders in Rest of the World, 2020-2030
13.7.1.5. Medical Device CRO Market for
Respiratory Disorders in Rest of the World, 2020-2030
13.7.1.6. Medical Device CRO Market for Pain Management Disorders in
Rest of the World, 2020-2030
13.7.1.7. Medical Device CRO Market for
Ophthalmic Disorders in Rest of the World, 2020-2030
13.7.1.8. Medical Device CRO Market for Psychological Disorders in
Rest of the World, 2020-2030
13.7.1.9. Medical Device CRO Market for
Metabolic Disorders in Rest of the World, 2020-2030
13.7.1.10. Medical Device CRO Market for Other Therapeutic Areas in Rest
of the World, 2020-2030
13.7.2. Medical Device CRO Market in Rest of
the World, 2020-2030: Distribution by Device Class
13.7.2.1. Medical Device CRO Market for Class I
Devices in Rest of the World, 2020-2030
13.7.2.2. Medical Device CRO Market for Class II
Devices in Rest of the World, 2020-2030
13.7.2.3. Medical Device CRO Market for Class
III Devices in Rest of the World, 2020-2030
13.7.3. Medical
Device CRO Market in Rest of the World, 2020-2030: Distribution by Type of Clinical
Service Offered
13.7.3.1. Medical Device CRO Market for Clinical
Trial Management Services in Rest of the World, 2020-2030
13.7.3.2. Medical Device CRO Market for
Consulting Services in Rest of the World, 2020-2030
13.7.3.3. Medical Device CRO Market for Data
Management Services in Rest of the World, 2020-2030
13.7.3.4. Medical Device CRO Market for
Regulatory Affairs Management Services in Rest of the World, 2020-2030
13.7.3.5. Medical Device CRO Market for Other
Clinical Services in Rest of the World, 2020- 2030
13.7.4. Medical
Device CRO Market in Rest of the World, 2020-2030: Distribution by Type of Preclinical
Service Offered
13.7.4.1. Medical Device CRO Market for Material
Characterization and Analytical Services in Rest
of the World, 2020-2030
13.7.4.2. Medical Device CRO Market for
Biocompatibility Testing Services in Rest of the World, 2020-2030
13.7.4.3. Medical Device CRO Market for
Sterility and Microbiology Testing Services in Rest of the World, 2020-2030
13.7.4.4. Medical Device CRO Market for Other Preclinical Services in
Rest of the World, 2020-2030
14. CASE
STUDY: IMPACT OF CORONAVIRUS OUTBREAK
14.1. Chapter Overview
14.2. Impact of Coronavirus Upsurge on
Medical Device Industry
14.3. Future Strategies and Action
Plans: A Bird’s Eye View
15. SWOT
ANALYSIS
15.1. Chapter Overview
15.2. Strengths
15.3. Weaknesses
15.4. Opportunities
15.5. Threats
15.6. Concluding Remarks
16. FUTURE
TRENDS AND OPPORTUNITIES
16.1. Chapter
Overview
16.2. Anticipated Growth in Number of Connected Devices
16.3. Adoption of Data Analytics and Real-Time Monitoring Solutions
16.4. Need for Cloud-based Computing and Storage Solutions
16.5. Growing
Need for Real World Evidence for Regulatory Approval
16.6. Concluding
Remarks
17. INTERVIEW
TRANSCRIPTS
17.1. Chapter
Overview
17.2. Lajos Sarosi,
Chief Executive Officer and Co-founder, HungaroTrial
17.3. Christopher Rupp, Vice President of
Global Marketing and Commercial Operations, NAMSA
17.4. Christian
Wolflehner, General Manager, CW Research & Management
17.5. Troy McCall,
Chief Operating Officer, CROMSOURCE
17.6. Nazish Urooj,
Senior manager, Medical & Clinical Operations, Metrics Research
17.7. C. Omprakash,
Technical Director and Partner, Vyomus Consulting
17.8. Tania Persson,
Director of Business Development, A+ Science
17.9. Alexa
Foltin-Mertgen, Business Development Manager, AtoZ-CRO
18. APPENDIX
1: TABULATED DATA
19. APPENDIX
2: LIST OF COMPANIES AND ORGANIZATIONS
Contact Details
Gaurav Chaudhary
+1 (415) 800 3415
