Market revenue in 2024 | USD 2,689.7 million |
Market revenue in 2030 | USD 4,478.1 million |
Growth rate | 8.9% (CAGR from 2024 to 2030) |
Largest segment | Product survellaince & rc |
Fastest growing segment | Complaint Log/Intake |
Historical data covered | 2018 - 2023 |
Base year for estimation | 2024 |
Forecast period covered | 2025 - 2030 |
Quantitative units | Revenue in USD million |
Market segmentation | Complaint Log/Intake, Product Survellaince & RC, Retuened Non-returned product analysis, Resolve & Closure |
Key market players worldwide | IQVIA Holdings Inc, Wipro Ltd ADR, FREYR Battery Inc, Honeywell International Inc, SAS, PAREXEL, Tata Consultancy Services, Biovia, MasterControl, AssurX |
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The databook is designed to serve as a comprehensive guide to navigating this sector. The databook focuses on market statistics denoted in the form of revenue and y-o-y growth and CAGR across the globe and regions. A detailed competitive and opportunity analyses related to medical device complaint management market will help companies and investors design strategic landscapes.
Product survellaince & rc was the largest segment with a revenue share of 56.27% in 2024. Horizon Databook has segmented the Europe medical device complaint management market based on complaint log/intake, product survellaince & rc, retuened non-returned product analysis, resolve & closure covering the revenue growth of each sub-segment from 2018 to 2030.
Europe’s medical device contract research organization market held the third-largest share in 2023. Europe is one of the leading regions with advanced technologies and well-established infrastructure, resulting in improved healthcare facilities and patient care.
Players seeking entry into the European market require extensive knowledge of regulatory procedures and services in various EU member states. Small and mid-sized medical device companies without a regulatory affairs department generally hire a regulatory consultant or a legal representative for assistance in the various stages of regulatory approval processes needed for product development in Europe.
The regulatory framework in the EU is expected to undergo major changes over the coming years, which may affect market access or scope of entry. The market is expected to grow lucratively due to stringent regulatory policies.
Horizon Databook provides a detailed overview of continent-level data and insights on the Europe medical device complaint management market , including forecasts for subscribers. This continent databook contains high-level insights into Europe medical device complaint management market from 2018 to 2030, including revenue numbers, major trends, and company profiles.
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