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
