Global Medical Device Testing and Certification Market - Growth, Trends, and Forecast (2020 - 2025) -

DUBLIN--()--The "Medical Device Testing and Certification Market - Growth, Trends, and Forecast (2020 - 2025)" report has been added to's offering.

Medical devices are subjected to comply with strict regulatory protocols, as it is vital to ensure the efficacy and safety of medical devices. Therefore, it is compulsory for every device to comply with national and international standards before entering a market. The standard guidelines of medical devices vary from country to country, and it is mandatory for every manufacturer to follow these guidelines for marketing or selling of their products in a country. For example, the United States follows FDA guidelines, Europe considers CE approval, Canada needs Health Canada Registration, and India requires approval from CDSCO. This diverse range of regulatory landscape drives the testing and certification market for aesthetic devices.

Since regulations are different in every country, it is crucial for each medical device manufacturer to register or receive regulatory guidelines of that specific country, which, in turn, indicates the need for authorized third-parties to register their devices. National regulatory authorities of every country prefer that the manufacturers selling their products in that particular country should comply with standard guidelines, and get it checked by a third-party certification system. This can result in propelling the testing and certification market, as well as increase easy market access. The other factors, such as increasing need of validation and verification (V&V) for medical devices are driving the medical device testing and certification market.

Key Market Trends

Testing Services are Expected to Witness Rapid Growth

Medical devices are regulated by various regulatory authorities and compliances. This is mainly because the end-users of these devices expect outstanding performance, effectiveness, and safety from these medical devices. Therefore, it is mandatory for the manufacturers to properly define and implement medical device testing strategy which makes the device effective and production becomes easier due to the confirmation of quality.

An effective medical device testing strategy needs several sets of test requirements. These test requirements are based on the component specification, manufacturing process, and other critical functional specifications of the device. Test requirements define and describe setup conditions, actions, and expected response constraints for each experiment defined in the test steps.

These sets of requirements are required to smoothen test implementation as tests are carried out continuously at different stages of the complete manufacturing process, from component selection to a final assembly of a medical device, and each stage has different requirements and different parameters to be satisfied.

Thus, increasing medical devices will also increase these testing services, which is expected to augment the growth of the market.

North America Dominates the Market

North America dominates the medical device testing and certification market due to the increased focus on the quality of the medical devices and the presence of a large number of companies that serve the medical device industry. In the North America region, the United States is having the largest share in the market and the country is expected to witness a similar trend over the forecast period due to the presence of well-developed healthcare and the presence of top multinatiional medical device companies.

Key Topics Covered:





4.1 Market Overview

4.2 Market Drivers

4.2.1 Increasing Need of Validation and Verification (V&V) for Medical Devices

4.2.2 Compliance of Standards

4.3 Market Restraints

4.3.1 Diversity in Regulation

4.4 Porter's Five Force Analysis

4.4.1 Threat of New Entrants

4.4.2 Bargaining Power of Buyers/Consumers

4.4.3 Bargaining Power of Suppliers

4.4.4 Threat of Substitute Products

4.4.5 Intensity of Competitive Rivalry


5.1 By Service Type

5.1.1 Testing Services

5.1.2 Inspection Services

5.1.3 Certification Services

5.1.4 Other Services

5.2 By Sourcing Type

5.2.1 In-House

5.2.2 Outsourced

5.3 By Device Class

5.3.1 Class I

5.3.2 Class II

5.3.3 Class III

5.4 By Technology

5.4.1 Active Implant Medical Device

5.4.2 Active Medical Device

5.4.3 Non-Active Medical Device

5.4.4 In-Vitro Diagnostic Medical Device

5.4.5 Ophthalmic Medical Device

5.4.6 Orthopedic and Dental Medical Device

5.4.7 Vascular Medical Device

5.4.8 Other Technologies

5.5 Geography

5.5.1 North America

5.5.2 Europe

5.5.3 Asia Pacific

5.5.4 Middle East and Africa

5.5.5 South America


6.1 Company Profiles

6.1.1 BSI Group

6.1.2 Dekra Testing and Certification GmbH

6.1.3 Eurofins Scientific

6.1.4 Institute for testing and Certification Inc.

6.1.5 Intertek Group PLC

6.1.6 SGS SA

6.1.7 TUV Rheinland

6.1.8 UL LLC


For more information about this report visit

Laura Wood, Senior Press Manager

For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

Laura Wood, Senior Press Manager

For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900