Medical Device CROs for Regulatory Affairs Management Market, 2019-2030

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A detailed discussion on the need for regulatory review / oversight across different stages of the medical devices supply chain

More than 130 medical devices were approved by the FDA since January 2018, while several are currently being evaluated across more than 9,500 (active) clinical trials, worldwide. Even though technical innovation has enabled the development of a variety of versatile medical devices, product approval, given stringent regulatory standards, is still a concern.


To order this 550+ page report, which features 245+ figures and 250+ tables, please visit this - https://www.rootsanalysis.com/reports/view_document/med-dev-regulatory/282.html


Key Market Insights

  • Over 400 companies claim to possess the required expertise to offer regulatory affairs management-related services to medical device-focused business entities
  • A detailed review of the current Medical Device CRO market landscape of the medical devices regulatory affairs outsourcing market, featuring a list of over 400 CROs engaged in this domain.
  • The market landscape is highly fragmented, featuring the presence of both established players and new entrants; majority of such firms are located in the developed geographies
  • Service providers are catering to a diverse clientele, enabling sponsors to compliance to the standards of both regional and international regulators
  • Owing to the high competition, companies involved in this domain are steadily expanding their capabilities in order to augment their respective service portfolios and comply to evolving industry benchmarks



The USD 820 million (by 2030) financial opportunity within the contract regulatory affairs-management services market for medical devices has been analyzed across the following segments:

  • Medical Device Class
  • Class I
  • Class II
  • Class III


  • Therapeutic Area
  • Cardiovascular Disorders
  • CNS Disorders
  • Metabolic Disorders
  • Oncological Disorders
  • Ophthalmological Disease
  • Orthopedic Disorders
  • Pain Disorders
  • Respiratory Disorders
  • Others


  • Type of Regulatory Affairs Service
  • Pharmacies GAP-Analysis
  • Pharmacies Legal Representation
  • Pharmacies Notified Body Selection
  • Product Labelling-related Services
  • Product Registration and Clinical Trial Applications
  • Regulatory Document Submissions
  • Regulatory Writing and Publishing
  • Risk Management-related Services
  • Technical Dossier Set-up
  • Vigilance Medical Device Report


  • Key Geographical Regions
  • North America
  • Europe
  • Asia-Pacific and Rest of the World


The Medical Device CROs Market, 2019-2030.”  report features the following companies, which we identified to be key players in this domain:

  • CTI Clinical Trial and Consulting Services
  • ICON
  • Intertek
  • Medpace
  • MIC Medical
  • North American Science Associates (NAMSA)
  • Parexel
  • PharmaLex
  • Premier Research 
  • Société Générale de Surveillance (SGS)
  • Underwriters Laboratory (UL)


Table of Contents


  1. Preface

    2. Executive Summary

  2. Introduction
  3. Role of Regulatory Affairs in Medical Device Supply Chain
  4. Regulatory and Reimbursement Landscape for Medical Devices
  5. Competitive Landscape
  6. Company Profiles
  7. Competitive Benchmarking
  8. Guide to Regulatory Outsourcing Models
  9. Medical Device Regulatory Affairs: Key Performance Indicators
  10. Market Forecast
  11. Conclusion
  12. Survey Insights
  13. Executive Insights


  1. Appendix 1: Tabulated Data


  1. Appendix 2: List of Companies and Organizations


To purchase a copy, please visit  https://www.rootsanalysis.com/reports/view_document/med-dev-regulatory/282.html  


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