The critical role of medical devices
can be understood from the fact that any component or software failure can put
the lives of patients in jeopardy. To ensure these devices function to their
optimum level on a consistent basis, they are subjected to a plethora of
regulations and compliances such as IEC 60601-xx, IEC 17025, ISO 14708-3, and
ISO 14971. In fact, the World Health Organization (WHO) has recommended to all
governments the need to set-up regulations for medical devices. This is to
assure all stakeholders of the ability of devices in offering necessary risk
mitigation and minimizing harm in case of any malfunction. As a result,
manufacturers have undertaken medical
device testing to check various components and embedded software within
such devices for enabling consistent performance.
The above requisites called for the medical
devices testing specialists to define and implement the right
testing strategy throughout the manufacturing process. To cite an example,
manufacturers should validate every functionality of the medical device right
from the concept and design phase for better test coverage. On the other hand,
should they test the manufactured devices for functionalities and identify
glitches therein, the cost of implementing solutions will be high and
time-consuming.
Medical
device testing identifies the risks and impact of
various environmental conditions and focuses on the reliability of devices
vis-a-vis the inputs. It involves various types of testing related to the
lifecycle, compliance, interoperability, reliability, and performance of
medical devices. Medical device
functional testing also focuses on risks concerning electrical,
mechanical, and environmental aspects. The medical devices testing experts conduct technical testing on the
subassemblies, components, and the finished product to ensure the latter’s
effectiveness.
Devising an
impactful strategy for medical device testing
The medical devices testing specialists should take inputs from the
design team to create test structures that conform to the software, hardware,
and other requirements. Moreover, the test requirements for devices are based
on the manufacturing process, component specifications, and other functional
specifications. These help manufacturers in carrying out tests throughout the manufacturing process - from selecting individual components to their final assemblage.
Practical approach
to medical device testing
Any practical strategy to test
medical devices should involve phases like analysis, design, deployment,
closure, and maintenance. To validate testing as per the test requirements and
parameters, the following types of testing are undertaken.
Microprocessor
testing: To conduct effective performance
testing of medical devices, they should be subjected to solid
electronic testing. Since most medical devices come with built-in
microprocessors, the test process should commence with microprocessor testing.
Importantly, medical devices
testing experts should execute such testing prior to the integration of
microprocessors to the Printed Circuit Boards (PCBs). Testing the transistors
and integrated circuits inside a microprocessor should consider their
interconnection and logic gate functions.
Post integrating the components to
the PCB, the QA team uses common defects of an assembly model and identifies
the wrong component, open interconnect, and missing component. Moreover, any
modern test equipment allows direct measurement of device components in small
units. However, care must be taken to ensure these components within the PCB
should not impact the functioning of the whole medical device. Even though
functional testing is a crucial part of the testing process, it does not
suffice to find other manufacturing defects. This necessitates additional
troubleshooting.
Test automation: This process is conducted by using an electronic system
comprising instruments, a computer, and software. While testing high-tech
medical devices with varying current and voltage requirements, the test team
might grapple with generating test cases and measuring their accuracy.
Interoperability: Testing medical devices should invariably check for the
interoperability of devices and applications to uphold data privacy and
security. The tests should be recorded for the purpose of audit and compliance.
With innovations involving the Internet of Things, there is a need for the
applications, devices, and controls to integrate with the software at the core.
Security: In today’s challenging digital scenario there is an
urgent need to make the embedded software within medical devices hack-proof.
These include adopting measures like firewall testing, encrypting the user
data, and the authentication and validation of user log-ins, among others. The security testing
of devices should aim at protecting the health information of patients and
ensure they adhere to the provisions of the Health Insurance Portability and
Accountability Act.
In addition to the above types of
testing, medical devices should be tested for regulations and compliance,
especially as per FDA. Finally, the practical approach to testing medical
devices should include GUI testing, performance testing, non-GUI testing,
compliance testing, interoperability testing, behavior testing, reliability testing,
and user acceptance testing.
Conclusion
A robust approach to testing medical
devices is critical to ensure their effectiveness. It can help manufacturers
from preempting situations like device recall and save money in retesting
devices should glitches be found. In an industry that requires stringent
adherence to quality, manufacturers should engage organizations with domain
knowledge and experience.
Author Bio
Oliver has been associated with Cigniti Technologies Ltd as an
Associate Manager - Content Marketing, with over 10 years of industry
experience as a Content Writer in Software Testing & Quality Assurance
industry. Cigniti is a Global Leader in Independent Quality Engineering &
Software Testing Services with CMMI-SVC v1.3, Maturity Level 5.
This article is originally published on medium.com
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