The market for Medical Device Validation & Verification was valued at US$ 495.72 million in 2021, and it is anticipated to increase to US$ 998.26 million by 2027, with a CAGR of 10.2% during 2022 and 2027.
International regulatory standards established by key authorities, such as the United States Food and Drug Administration (FDA), are continually evolving as a result of severe regulatory policies imposed by many countries. Medical equipment are getting smaller and more intricately designed as technology advances. As a result, the importance of medical device validation and verification has increased. This validation and verification method aids in the error-free design of medical equipment of the highest caliber. Verification and validation also lower the cost of producing medical equipment.
The demand for medical device validation and verification is rising as a result of the growing need for high-tech, high-quality medical devices and the complexity of product design and engineering. Additionally, the complexity and connection of medical devices have increased. The adoption of digital technology is simple and widespread throughout the healthcare industry. Because of the addition of software, medical equipment are becoming increasingly sophisticated. Previously, turning on and off the equipment and displaying information were done manually using the software in medical devices. The medical device software has become significantly more sophisticated as a result of the complexity of the requirements and customer requests, which has increased the need for validation and verification.
January 12, 2022: TÜV SÜD Announces Medical Device Testing Laboratory Expansion, Adding 26 High-Skilled Job Opportunities in New Brighton, MN--
TÜV SÜD announces its plans to expand its Medical & Health Services (MHS) facilities in New Brighton, Minnesota, during a groundbreaking ceremony. This 20,000 square foot laboratory extension of its existing 36,000 square foot test facility to be completed by June 2022 will offer an end-to-end testing solution for all medical devices.
Market is segmented based on the type, applications, companies and regions.
By Type, it is segmented into
By Application, it is segmented into
Due to recent technical breakthroughs in medical devices and increased complexity in product design, North America held the greatest share of 44.88% in 2019. Additionally, because the healthcare sector is flourishing in North America, producers of medical devices are concentrating there. North America is therefore expected to control the global market over the estimate.
In 2019, Europe accounted for the second-largest share of the worldwide market thanks to its highly developed healthcare system. Due to rising regulatory emphasis on quality control during medical device production, particularly in emerging nations like China and India, the Asia Pacific region is anticipated to hold a sizable market share over the course of the projected period. In addition, the market in the Asia Pacific is anticipated to be driven by rising medical tourism in emerging economies. Due to the rapidly expanding healthcare business, some regions, including the Middle East and Africa and Latin America, are predicted to have profitable growth in the near future.
The Medical Device Validation & Verification Market describes the factors driving the global growth opportunities in upcoming years and highlights market channels. In addition, the report analyzes market size and share, trends, by geographic region, end-use type and segment. It focuses extensively on revealing a detailed regional analysis. The Global Medical Device Validation & Verification Market report also conducted a PESTEL analysis of the industry to study the main influencing factors and entry barriers of the industry.
Report Attributes | Report Details |
Forecast Period 2022 to 2027 CAGR | CAGR of 10.2% over the forecast period (2022-2027) |
By Type |
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By Application |
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By Companies | SGS SA, QuEST Global Services Pte. Ltd, Intertek, Element Materials Technology, TÜV SÜD AG, North American Science Associates, Inc. (NAMSA), Eurofins Scientific SE, Charles River, Sterling Medical Devices, Pacific Biolabs, Toxikon Corporation, Steris Laboratories, Global Services Pte., Ltd, NAMSA |
Regions Covered |
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Countries Covered |
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Base Year | 2022 |
Historical Year | 2017 to 2021 |
Forecast Year | 2022 to 2027 |
Number of Pages | 137 |
Customization Available | Yes, the report can be customized as per your needs |
What is the growth rate of Medical Device Validation & Verification Market?
The Medical Device Validation & Verification Market is growing at a CAGR of 10.2% over the next 5 years.
Who are the key players in Medical Device Validation & Verification Market?
SGS SA, QuEST Global Services Pte. Ltd, Intertek, Element Materials Technology, TÜV SÜD AG, North American Science Associates, Inc. (NAMSA), Eurofins Scientific SE, Charles River, Sterling Medical Devices, Pacific Biolabs, Toxikon Corporation, Steris Laboratories, Global Services Pte., Ltd, NAMSA
What are the significant types of Medical Device Validation & Verification Market?
Diagnostics, Therapeutic, Implants
What are the major end-use applications of Medical Device Validation & Verification Market?
Cardiovascular, Dermatology, Orthopedics, Nephrology, Respiratory, Neurology, Oncology, ENT, Others
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SECONDARY RESEARCH
Secondary Research Information is collected from a number of publicly available as well as paid databases. Public sources involve publications by different associations and governments, annual reports and statements of companies, white papers and research publications by recognized industry experts and renowned academia etc. Paid data sources include third party authentic industry databases.
PRIMARY RESEARCH
Once data collection is done through secondary research, primary interviews are conducted with different stakeholders across the value chain like manufacturers, distributors, ingredient/input suppliers, end customers and other key opinion leaders of the industry. Primary research is used both to validate the data points obtained from secondary research and to fill in the data gaps after secondary research.
MARKET ENGINEERING
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EXPERT VALIDATION
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REPORT WRITING/ PRESENTATION
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