Test and Validate the Quality of Your Medical Devices with Performance Testing
Performance testing is critical in the design, development and compliance process for medical devices. It involves evaluating a device to ensure that it meets predefined standards, functions as intended, and performs safely and reliably under expected conditions. This testing assesses various aspects of the device, including its functionality, reliability, and safety.
Functional testing ensures that the device performs its primary functions as intended, while reliability testing verifies its consistency over time and across different environments. Stress and environmental testing determine how the device behaves under extreme conditions, such as high temperatures or humidity. Additionally, biocompatibility testing ensures that materials used in the device are safe for human contact, and regulatory compliance testing confirms that the device meets the requirements of agencies like the FDA or ISO.
Benefits of Performance Testing for Medical Devices
The benefits of performance testing are numerous. It significantly improves patient safety by identifying and mitigating potential risks or failures before the device reaches the market. It also helps secure regulatory approval by demonstrating that the device meets industry standards, expediting the approval process. Moreover, performance testing enhances the reliability of the device, ensuring that it functions consistently in diverse conditions. This, in turn, minimizes the risk of product liability issues, such as lawsuits or recalls.
Performance testing also strengthens a device’s competitiveness in the market by showcasing its quality and reliability. It contributes to cost efficiency by identifying issues early in the process, which is much less expensive than handling failures after the device has been released.
Intertek's Solutions for Medical Device Performance Testing
In today’s healthcare market, your team must employ cutting edge technology to challenge the competition. Intertek offers a wide scope of custom performance testing services that help you assess risk and avoid costly field failures. We test well beyond mandatory requirements to determine the effects of certain stresses during your device’s life cycle, helping you to improve efficiencies in your development process and bring your product to market faster.
Battery Safety Testing for Medical Devices
Intertek provides Battery Safety Testing to the Requirements of IEC 62133 for Medical Devices throughout global markets with over 50 years of experience.
Reese's Law – ANSI/UL 4200A-2023
Reese’s Law (ANSI/UL 4200A-2023) has placed safety requirements on consumer products containing button cell or coin batteries in a significant stride towards enhancing child safety.
Home Healthcare Equipment Testing and Certification
Intertek offers comprehensive Testing and Certification solutions for Home Healthcare Equipment to all applicable standards including IEC 60601-1-11.
Accelerated Stress Testing for Medical Devices
Accelerated Stress Testing (AST) from Intertek can save time and lead to quality improvements of your medical devices, helping get you to market faster
Accelerated Reliability Testing
Through Accelerated Reliability Testing Intertek works with you to help uncover design defects or weaknesses that may not have been realized during product design
HALT Testing & HASS Testing
Discover the power of Intertek's Highly Accelerated Life Test (HALT) Testing: a rigorous method designed to push products to their limits, uncovering weaknesses and enhancing reliability.
Benchmark and Comparison Testing
Intertek offers tailor-made Benchmark and Comparison Testing solutions which will help you assess how your products perform against your competition.
Knowledge Center
Download the latest information from our medical device compliance experts
Creation of IEC 60601-1 4th Edition
IEC 60601-1-2 Ed. 4.1 Overview of Requirements
Medical OEM Wireless Coexistence Testing
Artificial Intelligence (AI) and Machine Learning (ML) in Medical Devices
Biocompatibility Risk Assessment and Evaluation Plans
For more expert papers, recordings, and presentations, visit our Medical Resources hub.
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** The Intertek legal entities that provide medical device management system certification services (including ISO 13485 and MDSAP) and Notified Body services (MDR 2017/745 and MDD 93/42/EEC) do not provide any consulting services. Clients who have used other Intertek legal entities’ consulting services are not eligible to receive management system certification services or Notified Body services from Intertek.