Effective Tips to Better Manage Medical Device Software Testing

It’s hard to recall a time when software wasn’t standard in electronic medical devices. Creating safe, issue-free software is a critical aspect when developing new devices. As such, it’s no surprise that medical device software testing is vital to a device’s eventual development success and sustainability.

Software testing is more involved for medical device software than in other industries. In comparison to other industries, the consequences of a software glitch or bug is greater for medical devices. As such, testing software in a medical device requires a thorough, rigorous, and exhaustive approach.

These stakes, and accompanying compliance regulations, require stricter, more thorough practices when performing testing on medical device software that can be challenging to manage.

Testing medical device software is deeply complex and must comply with more regulations than most other industries require for their software. A strong knowledge of the medical industry—as well as best practices for software testing is necessary to ensure a medical device is safe for use.

What you’ll find in this article:

What is medical device software testing?
The importance of testing software for medical devices.
Challenges of medical device software testing
How to manage medical device software challenges effectively

What is Medical Device Software Testing?

Medical device software testing is the process of evaluating and validating software used in medical devices to ensure it functions correctly, safely, and effectively. This testing is critical because any malfunction or defect in the software can directly impact patient health and safety.

Software testing for a medical device is different from software testing practices for non-medical devices; developers need a different approach when testing software for use in the medical industry.

Key differences between standard software testing practices and ones for testing software in a medical device often are:

Patient safety: The primary focus of medical device software testing is to ensure patient safety. This necessitates more thorough and extensive testing compared to standard software to identify and mitigate potential risks.
Regulatory compliance: Medical device software must comply with strict regulatory standards such as FDA guidelines, ISO 13485, and IEC 62304.
Validation and verification: Medical device software testing involves both verification (ensuring the product meets design specifications) and validation (ensuring the product meets user needs and intended use).
Clinical environment testing: Medical device software often requires testing in real-world clinical settings or simulated environments to ensure it performs correctly under actual usage conditions.
Risk management: Comprehensive risk management strategies are required to identify, assess, and mitigate potential risks throughout the software development lifecycle.
Traceability: In medical device software testing, every requirement, test case, and defect must be traceable back to specific regulatory and design requirements. This ensures complete accountability and compliance.
Usability testing: Medical device software must undergo usability testing to ensure it is safe and effective for healthcare professionals and patients.

The Importance of Testing Software for Medical Devices

Testing software for use in medical devices is a more involved and nuanced process than for other types of software. As mentioned earlier, medical device software is inherently risky due to its direct impact on patient health, stringent regulatory requirements, and the complexity of integrating with medical devices.

For instance, if an issue in the software of an insulin pump occurred, disrupting its ability to accurately monitor its user’s insulin and glucose levels, serious health concerns could quickly develop. With over 350,000 insulin pumps in use in the US, the potential impact of software failures on patient health is significant, highlighting the critical need for rigorous testing.

Here’s why medical device software testing is important.

Patient Safety

Any malfunction or bug can lead to incorrect diagnoses or treatment, potentially causing harm to patients.

Thoroughness in software testing ensures medical devices can be reliable in critical situations, such as the continuous operation of a ventilator pump or pacemaker monitoring. This reduces the risk of device failure during use, which we know can have severe consequences for patient health and safety.

Regulatory Compliance

Regulatory compliance is crucial for medical device software to be legally marketed and used. The rigorous software testing measures are in place to protect patient safety as well as meet established standards and regulatory requirements, avoiding costly recalls, and reducing the risk of data breaches and legal issues.

Key aspects of regulatory compliance of medical device software testing include:

Standards adherence: Ensuring alignment with ISO 13485, IEC 62304, and FDA guidelines.
Certification: Facilitating the certification process for market approval.
Documentation: Providing thorough documentation to demonstrate compliance during audits.

Device Performance

Medical device software testing ensures that the software operates efficiently and effectively, aligns with the device’s intended use, and that it performs all intended tasks without glitches. This leads to more reliable and accurate medical devices, crucial for patient care.

Furthermore, thorough testing improves the user experience for healthcare professionals and patients. By identifying and resolving potential issues early, testing ensures that medical devices are intuitive and easy to use, ultimately supporting better healthcare delivery and outcomes.

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Challenges of Medical Device Software Testing

Medical device software testing comes with unique challenges that can significantly impact the successful development of a medical device and its FDA approval. Common software testing challenges that medical device manufacturers often face include:

Meeting Compliance Requirements

Software in medical devices is required to meet the safety, security, and quality control regulations found in a number of regulatory bodies. Compliance requirements will depend on the type of software being tested, the class of the medical device it’s developed for, safety parameters, and the region the device will be used in.

Examples of regulations medical device software may be tested against include:

IEC 62304
ISO 13485
IEC 60601
ISO 14971

Lengthy Product Development Times

On average, 3 – 7 years is how long it takes to bring a new medical device to market. The extensive time required to meet all testing requirements can significantly slow down time to market launches.

Each phase, from regulatory compliance to real-time performance testing, demands thorough attention to detail and exhaustive documentation.

This prolonged testing period, while essential for ensuring safety and efficacy, can delay product launches and increase a device’s development costs. Balancing thorough testing with efficient time management is a key challenge for medical device manufacturers.

Interoperability

Ensuring interoperability is a significant challenge in medical device software testing. A medical device’s software must seamlessly integrate with various other medical systems and devices, such as:

Electronic Health Records (EHR) systems
Hospital information systems
Diagnostic equipment
Other therapeutic devices

Achieving this often involves using different communication protocols and data formats, all of which need thorough, rigorous testing processes to confirm their compatibility and functionality across diverse platforms.

Hardware Integrations

Electronic medical devices must physically interact with the patients they serve and care for, software alone cannot create these effects. As such, software for medical devices must integrate with a device’s physical components with great precision.

The software must interact flawlessly with sensors, processors, and other electronic components to ensure accurate and reliable performance of the device. Any discrepancies can lead to malfunctions, compromising patient safety.

Rigorous testing is required to verify that the software can handle various hardware configurations and operating conditions.

Other articles on medical device development:

Cybersecurity Risk Management

Testing software for cybersecurity and risk management is particularly challenging in medical device software due to the personal nature of the data it will handle, the compliance requirements they must adhere to, and the ever-evolving cybersecurity threat landscape.

Key challenges facing software testing teams of medical device software:

FDA approval: Medical device software must meet the unique risk management compliance requirements outlined in the FDA’s Cybersecurity in Medical Devices document.
Long-term security management. Regular testing is required to ensure a device’s software is safe from new or persistent threats and that potential threats can be easily identified and resolved before a device’s vulnerability can be exploited.

How to Manage Medical Device Software Testing Effectively: Partner with Vantage MedTech

Navigating medical device software testing is a daunting, albeit necessary, part of the medical device testing and development process.

When ensuring a device’s software is secure, safe for patients, and meets all necessary compliance requirements, there is no room for compromise. However, it’s not a simple process and requires time, attention to detail, and a strong knowledge foundation.

How do we know? At Vantage MedTech, we help large OEMs and start up companies manage their medical device software testing needs with ease. We help our clients to overcome:

Compliance Complexities

With Vantage MedTech, companies can access our extensive regulatory expertise, ensuring software testing practices meet necessary standards such as ISO 13485, IEC 62304, and others required by the FDA.

Lengthy Development Times

Our proprietary AdvantagePlatforms® significantly reduce development timelines by up to 60%, without compromising on quality or compliance needs. These customizable, pre-existing platform systems accelerate every medical device’s software testing process, ensuring faster time-to-market.

Hardware and Software Optimization Hurdles

Create precise alignment between a device’s software and hardware with help from our expert engineering team. We ensure flawless integrations between software and hardware components and provide rigorous testing to verify software performance and reliable device functionality.

Cybersecurity Risks

Your innovations are invaluable and deserve to be shielded from cyber threats. That’s where we come in. Our tailored medical device security solutions are designed to safeguard medical innovations.

We start off by developing the correct cybersecurity risk documentation – the first time – so your device stays compliant and secure in today’s healthcare environment.