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The quality and reliability of Bluetooth enabled devices is important and testing manually is time consuming, prone to errors and expensive. Automation of Bluetooth testing improves quality and reliability, while reducing costs. The Bluetooth Testing Framework supports the automation of testing Bluetooth enabled devices.

Test reporting is a key component of the test management process. Test reporting highlights the effectiveness of the testing efforts and provides valuable insights into the quality of the software being tested.

Test matrix and test metrics are essential components of the test management process. Each plays a unique role in ensuring the effectiveness of the testing efforts and providing valuable insights into the quality of the software being tested.

Requirements are the Key to developing a successful Software Project with the help of Quality Assurance.

Discover the blueprint for successful testing: From planning to execution, learn about the key elements and success factors of a Test Concept.

Acceptance Testing is a huge concern for Cyber Security during deployment of updates to the live system in the Demilitarised Zone (DMZ). Test Architecture, Test Environment and particularly Test Data must be considered. These must not be left open to attack, allowing access to the live system.

Testing is an important strategy for Cyber Security. There are a number of topics which must be considered to reduce the possibility of cyber intrusions into your systems via test environments.

Software Quality is an important component of cyber security and makes you better prepared for possible problems. Good quality software is more resilient against cyber-attacks.

Swissmedic, the Swiss Agency for Therapeutic Products, is involved in the entire life cycle of a medicinal products because of its mandated areas of responsibility in the sectors of licensing and the authorisation and monitoring of medicinal products. It is involved in the legal aspects of the process.

Across industries, standards are an important way to safeguard product conformity while simultaneously harmonizing requirements both nationally and internationally. Quality assurance is vital to ensure that the producer correctly applies standards.

GAMP® 5 provides pragmatic and practical industry guidance to achieve compliant computerized systems fit for intended use in an efficient and effective manner. Good Automated Manufacturing Practice (GAMP 5 ®) sets out principles and procedures that help ensure that pharmaceutical or medical device products have the required quality and details a recognized standard for Computer system validation (CSV).

Is your software development process healthy? Find out for free with our Software QA Health Check!

Discover the impact of Artificial Intelligence (AI) on Testautomation in software development. Read our latest article on meinTest.software to learn how AI is changing the way software is tested and how SmartBear's TestComplete is providing an innovative solution to improve the quality and speed of software testing. Find out how AI-supported tools are detecting errors early on and saving time for test engineers.

Companies can really benefit from implementing an independent QA audit based on TMMI, CMMI and itsbusiness AG have more than 20 years’ experience in different industries.
Performing an audit and implementing the recommendations will result in improvements in the Process and reduce Risk for software development.

Are you looking to save on costs, while improving the software quality of your comms enabled medical/sensor/drone device? If yes, then see how this can be done in our blog post on Hardware-in-the-Loop Testing.

In the pharmaceutical industry, good practices are an important way to safeguard product conformity and safety. Quality assurance is vital to ensure that the producer correctly applies good practices.

Standards are the vital keystone upon which safely functioning medical devices are built. Across industries, standards are an important way to safeguard product conformity. Standards harmonize requirements both nationally and internationally. Our whitepaper covers the Standards applied to the development of Software for Medical Devices. It highlights the most important points for Software Quality.

Usability is a key component of safety for medical device usage, and a clear and understandable user interface is vital. The standard which covers this is IEC 62366.

The Quality Management System is the backbone on which the development of safe medical devices is built. The standard which covers this is ISO 13485.

ISO standard ISO 14971 is used for the application of risk management to medical devices. This standard was developed specifically for manufacturers of medical devices on the basis of established principles of risk management that have evolved over many years.

Across industries, standards are an important way to safeguard product conformity while simultaneously harmonizing requirements both nationally and internationally. Quality assurance is vital to ensure that the producer correctly applies standards.

In the pharmaceutical industry, good practices are an important way to safeguard product conformity and safety. Quality assurance is vital to ensure that the producer correctly applies good practices.

Are you concerned about ensuring the stability of your Bluetooth-enabled device? If so, check out our latest blog entry on how our Bluetooth Testing Framework can help you automate testing and produce more reliable Bluetooth-enabled devices.

During development of medical devices, software standard IEC 62304 must be followed, and regression testing is a vital part of the Quality Assurance process.

Medical devices and associated software are heavily regulated.  The international standard IEC 62304– medical device software – software life cycle processes is a standard which specifies life cycle requirements for the development of medical software and software within medical devices.