In adopting a software process model, many small software companies are ignoring standard process models and models for process improvement. This study uses an empirical approach to investigate what processes software ...

Traditional software configuration management tools employ existing Diff tools to identify the difference between intermediate versions of a document such as a source code file. When any new data structure arises, developers ...

In an industrial context all process models require a certain amount of tailoring to fit to the business environment of any specific organization in which the model is to be deployed. Process models should therefore be ...

Increasingly medical devices are being designed to allow them to exchange information over an IT network. However incorporating a medical device into an IT network can introduce risks which can impact the safety, effectiveness ...

Medical device security is a growing concern for medical device manufacturers, healthcare delivery organisations and regulators in the industry. Increasingly, researchers are demonstrating exactly how vulnerable these ...

Medical devices are designed and produced subject to various standards. These standards are recognized by the regulatory authorities within the region in which they are going to be marketed. Traditionally medical devices ...

Medical Devices are widely used in patient care for both diagnosis and treatment purposes. Typically, modern medical devices are intended to be networked at their point of use. The incorporation of medical devices opens ...

The provision of care to patients has moved away from episodic acute care due to the increase in chronic diseases such as diabetes. This has changed the relationship between the patient and the care team. The management ...

Mobile medical apps are a growing mechanism for healthcare delivery through an increasingly complex network of information technology systems connecting patients, doctors, nurses, pharmacists and medical devices. ...

Medical device standards outline the requirements for developing medical devices. These standards, however, do not outline how these requirements should be implemented causing difficulties for organisations entering the ...