Global Medical Device Regulation (MDR) Certification Service Market Growth (Status and Outlook) 2024-2030

Global Medical Device Regulation (MDR) Certification Service Market Growth (Status and Outlook) 2024-2030

Medical Device Regulation (MDR) certification services refer to services that evaluate and certify medical device products according to the European Union's Medical Device Regulation. MDR certification is one of the legal requirements for medical devices sold on the European market. It aims to ensure that the safety and performance of medical devices comply with the standards and regulatory requirements of the European market. EU MDR 2017/745 comes into force in May 2021 . All medical devices certified under the previous Medical Devices Directive (MDD) must be certified in accordance with the new requirements to ensure they can continue to be marketed in Europe.The EU MDR 2017/745 came into effect in May 2021. All medical devices certified under the previous Medical Device Directive (MDD) must certify to the new requirements to ensure that they can continue to be sold in the European market.

The global Medical Device Regulation (MDR) Certification Service market size is projected to grow from US$ million in 2024 to US$ million in 2030; it is expected to grow at a CAGR of %from 2024 to 2030.

LPI (LP Information)' newest research report, the “Medical Device Regulation (MDR) Certification Service Industry Forecast” looks at past sales and reviews total world Medical Device Regulation (MDR) Certification Service sales in 2022, providing a comprehensive analysis by region and market sector of projected Medical Device Regulation (MDR) Certification Service sales for 2023 through 2029. With Medical Device Regulation (MDR) Certification Service sales broken down by region, market sector and sub-sector, this report provides a detailed analysis in US$ millions of the world Medical Device Regulation (MDR) Certification Service industry.

This Insight Report provides a comprehensive analysis of the global Medical Device Regulation (MDR) Certification Service landscape and highlights key trends related to product segmentation, company formation, revenue, and market share, latest development, and M&A activity. This report also analyses the strategies of leading global companies with a focus on Medical Device Regulation (MDR) Certification Service portfolios and capabilities, market entry strategies, market positions, and geographic footprints, to better understand these firms’ unique position in an accelerating global Medical Device Regulation (MDR) Certification Service market.

This Insight Report evaluates the key market trends, drivers, and affecting factors shaping the global outlook for Medical Device Regulation (MDR) Certification Service and breaks down the forecast by Type, by Application, geography, and market size to highlight emerging pockets of opportunity. With a transparent methodology based on hundreds of bottom-up qualitative and quantitative market inputs, this study forecast offers a highly nuanced view of the current state and future trajectory in the global Medical Device Regulation (MDR) Certification Service.

United States market for Medical Device Regulation (MDR) Certification Service is estimated to increase from US$ million in 2023 to US$ million by 2030, at a CAGR of % from 2024 through 2030.

China market for Medical Device Regulation (MDR) Certification Service is estimated to increase from US$ million in 2023 to US$ million by 2030, at a CAGR of % from 2024 through 2030.

Europe market for Medical Device Regulation (MDR) Certification Service is estimated to increase from US$ million in 2023 to US$ million by 2030, at a CAGR of % from 2024 through 2030.

Global key Medical Device Regulation (MDR) Certification Service players cover TÜV Rheinland, DQS, Intertek, DEKRA, SGS Société Générale de Surveillance SA, etc. In terms of revenue, the global two largest companies occupied for a share nearly % in 2023.

This report presents a comprehensive overview, market shares, and growth opportunities of Medical Device Regulation (MDR) Certification Service market by product type, application, key players and key regions and countries.

Segmentation by Type:
Assessment and Certification Services
Training、Assessment and Certification Services
Others

Segmentation by Application:
Manufacturers of Medical Devices
Authorized Representatives of Medical Devices
Importers and Distributors of Medical Devices
Research and Development Organizations and Medical Innovation Companies
Others

This report also splits the market by region:
Americas
United States
Canada
Mexico
Brazil
APAC
China
Japan
Korea
Southeast Asia
India
Australia
Europe
Germany
France
UK
Italy
Russia
Middle East & Africa
Egypt
South Africa
Israel
Turkey
GCC Countries

Segmentation by Type:
Assessment and Certification Services
Training、Assessment and Certification Services
Others

Segmentation by Application:
Manufacturers of Medical Devices
Authorized Representatives of Medical Devices
Importers and Distributors of Medical Devices
Research and Development Organizations and Medical Innovation Companies
Others

This report also splits the market by region:
Americas
United States
Canada
Mexico
Brazil
APAC
China
Japan
Korea
Southeast Asia
India
Australia
Europe
Germany
France
UK
Italy
Russia
Middle East & Africa
Egypt
South Africa
Israel
Turkey
GCC Countries

The below companies that are profiled have been selected based on inputs gathered from primary experts and analyzing the company's coverage, product portfolio, its market penetration.
TÜV Rheinland
DQS
Intertek
DEKRA
SGS Société Générale de Surveillance SA
RISE
BSI
DNV MEDCERT GmbH
Eurofins
ITC ZLÍN
3EC International
CE Certiso
Certiquality
IMQ
Kiwa

Please note: The report will take approximately 2 business days to prepare and deliver.