< Key Hightlight >
The United States Medical Device Validation & Verification Market size was estimated at USD 136.22 million in 2020 and expected to reach USD 148.29 million in 2021, at a CAGR 10.47% to reach USD 247.69 million by 2026.
Market Statistics:
The report provides market sizing and forecast across five major currencies - USD, EUR GBP, JPY, and AUD. It helps organization leaders make better decisions when currency exchange data is readily available. In this report, the years 2018 and 2019 are considered historical years, 2020 as the base year, 2021 as the estimated year, and years from 2022 to 2026 are considered the forecast period.
Market Segmentation & Coverage:
This research report categorizes the Medical Device Validation & Verification to forecast the revenues and analyze the trends in each of the following sub-markets:
Based on Therapeutic Area, the market was studied across Cardiovascular, Dermatology, ENT, Nephrology, Neurology, Oncology, Orthopedics, and Respiratory.
Based on Application, the market was studied across Diagnostics, Implants, and Therapeutic. The Implants is further studied across Active Implantable Medical Device and Medical Implants.
Based on Technology, the market was studied across Biological, Electrical safety testing, EMC/ECI, and Mechanical testing.
Based on State, the market was studied across California, Florida, Illinois, New York, Ohio, Pennsylvania, and Texas.
Cumulative Impact of COVID-19:
COVID-19 is an incomparable global public health emergency that has affected almost every industry, and the long-term effects are projected to impact the industry growth during the forecast period. Our ongoing research amplifies our research framework to ensure the inclusion of underlying COVID-19 issues and potential paths forward. The report delivers insights on COVID-19 considering the changes in consumer behavior and demand, purchasing patterns, re-routing of the supply chain, dynamics of current market forces, and the significant interventions of governments. The updated study provides insights, analysis, estimations, and forecasts, considering the COVID-19 impact on the market.
Competitive Strategic Window:
The Competitive Strategic Window analyses the competitive landscape in terms of markets, applications, and geographies to help the vendor define an alignment or fit between their capabilities and opportunities for future growth prospects. It describes the optimal or favorable fit for the vendors to adopt successive merger and acquisition strategies, geography expansion, research & development, and new product introduction strategies to execute further business expansion and growth during a forecast period.
FPNV Positioning Matrix:
The FPNV Positioning Matrix evaluates and categorizes the vendors in the Medical Device Validation & Verification Market based on Business Strategy (Business Growth, Industry Coverage, Financial Viability, and Channel Support) and Product Satisfaction (Value for Money, Ease of Use, Product Features, and Customer Support) that aids businesses in better decision making and understanding the competitive landscape.
Market Share Analysis:
The Market Share Analysis offers the analysis of vendors considering their contribution to the overall market. It provides the idea of its revenue generation into the overall market compared to other vendors in the space. It provides insights into how vendors are performing in terms of revenue generation and customer base compared to others. Knowing market share offers an idea of the size and competitiveness of the vendors for the base year. It reveals the market characteristics in terms of accumulation, fragmentation, dominance, and amalgamation traits.
Competitive Scenario:
The Competitive Scenario provides an outlook analysis of the various business growth strategies adopted by the vendors. The news covered in this section deliver valuable thoughts at the different stage while keeping up-to-date with the business and engage stakeholders in the economic debate. The competitive scenario represents press releases or news of the companies categorized into Merger & Acquisition, Agreement, Collaboration, & Partnership, New Product Launch & Enhancement, Investment & Funding, and Award, Recognition, & Expansion. All the news collected help vendor to understand the gaps in the marketplace and competitor’s strength and weakness thereby, providing insights to enhance product and service.
Company Usability Profiles:
The report profoundly explores the recent significant developments by the leading vendors and innovation profiles in the United States Medical Device Validation & Verification Market, including Bressler group, Celestica Inc., Charles River Laboratories Inc., Cigniti Technologies Limited, Eurofins Scientific SE, F. Hoffmann-La Roche Ltd, Fluke Corporation, Intertek Group PLC, Jabil Inc, Johnson & Johnson Services, Inc., Nordson Corporation, Pacific BioLabs, Inc., Plexus Corp., QuEST Global Services Pte. Ltd, SGS SA, StarFish Product Engineering Inc., Sterigenics U.S., LLC, Sterislabs Inc, Sterling Medical Devices, Inc, The General Electric Company, TÜV SÜD AG, and Ximedica, LLC.
The report provides insights on the following pointers:
1. Market Penetration: Provides comprehensive information on the market offered by the key players
2. Market Development: Provides in-depth information about lucrative emerging markets and analyze penetration across mature segments of the markets
3. Market Diversification: Provides detailed information about new product launches, untapped geographies, recent developments, and investments
4. Competitive Assessment & Intelligence: Provides an exhaustive assessment of market shares, strategies, products, certification, regulatory approvals, patent landscape, and manufacturing capabilities of the leading players
5. Product Development & Innovation: Provides intelligent insights on future technologies, R&D activities, and breakthrough product developments
The report answers questions such as:
1. What is the market size and forecast of the United States Medical Device Validation & Verification Market?
2. What are the inhibiting factors and impact of COVID-19 shaping the United States Medical Device Validation & Verification Market during the forecast period?
3. Which are the products/segments/applications/areas to invest in over the forecast period in the United States Medical Device Validation & Verification Market?
4. What is the competitive strategic window for opportunities in the United States Medical Device Validation & Verification Market?
5. What are the technology trends and regulatory frameworks in the United States Medical Device Validation & Verification Market?
6. What is the market share of the leading vendors in the United States Medical Device Validation & Verification Market?
7. What modes and strategic moves are considered suitable for entering the United States Medical Device Validation & Verification Market?
Bressler group
Celestica Inc.
Charles River Laboratories Inc.
Cigniti Technologies Limited
Eurofins Scientific SE
F. Hoffmann-La Roche Ltd
Fluke Corporation
Intertek Group PLC
Jabil Inc
Johnson & Johnson Services, Inc.
Nordson Corporation
Pacific BioLabs, Inc.
Plexus Corp.
QuEST Global Services Pte. Ltd
SGS SA
StarFish Product Engineering Inc.
Sterigenics U.S., LLC
Sterislabs Inc
Sterling Medical Devices, Inc
The General Electric Company
TÜV SÜD AG
Ximedica, LLC
California
Florida
Illinois
New York
Ohio
Pennsylvania
Texas