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Making Software Quality
an Inherent Part of Medical Device R&D

As the proportion of software in medical devices continues to rise, quality, safety, and compliance are no longer supplementary tasks in the later stages of R&D, but core capabilities that span the entire product lifecycle.
As the authorized agent and industry solution partner for Parasoft software in China, Glyph Translation (Shenzhen) Co., Ltd.
is committed to introducing internationally leading software testing and continuous quality concepts into medical device R&D practices, helping enterprises systematically meet quality and compliance requirements while improving development efficiency.

Software Test Automation

Medical Device Software Quality and Compliance Support

IEC 62304 Lifecycle-Based Approach

Learn About Software Solutions Contact Us

Founded in 1987 and headquartered in Los Angeles, California, USA, Parasoft is a leading global provider of automated software testing, static analysis, and continuous quality solutions.

For over 30 years, Parasoft has consistently served industries with extremely high requirements for software safety, reliability, and compliance, including medical devices, aerospace and defense, automotive and industrial control, energy, and critical infrastructure.

Currently, Parasoft serves over 25,000 enterprise customers, including 88% of the Fortune World 100. Its continuous quality platform is widely used in the development of safety-critical software and the establishment of compliance frameworks.

Real-World Challenges in Medical Device Software R&D

01

Continuous growth in software scale and complexity
02

Manual testing struggles to cover all risks
03

Disconnect between quality activities and R&D workflows
04

Clear compliance requirements, but high costs of implementation and demonstrating compliance

The Value of Glyph Translation (Shenzhen) Co., Ltd.

As Parasoft's authorized agent and industry solution partner in China, we provide not only software licensing but also focus on:

01

Solution planning integrated with medical device R&D workflows
02

Assisting in the implementation of tools within R&D and quality systems
03

Assisting in the implementation of tools within R&D and quality systems
04

Helping to bridge software quality data with compliance documentation systems

Early identification of potential defects and safety risks
Support for standards such as MISRA, CERT, and CWE
Applicable to embedded and safety-critical software

Automated generation and execution of unit tests
Visualization of coverage data
Support for IEC 62304 software verification requirements

Automation of API and functional testing
Service virtualization to reduce environmental dependencies
Support for complex system integration validation

Aggregation of testing and quality data
Establishment of requirements-to-code-to-test traceability
Support for compliance audits and internal inspections

Code-level quality analysis
Unit and module-level validation
System and interface testing
Quality data aggregation and compliance reporting

Be Fully Prepared Linguistically for Every Critical Meeting

Software is becoming a core component of medical devices.
When software determines product performance and safety, quality and compliance must become part of the development process. Parasoft provides an internationally leading software testing and continuous quality platform, and Glyph Translation (Shenzhen) Co., Ltd. is committed to steadily introducing this capability into China's medical device industry.
The client roles we serve include: Heads of medical device software R&D; Heads of quality and validation; Regulatory and registration management teams

Contact Us to Learn More