Including Utilizing TensorFlow, Google's Open Source Library

The healthcare industry is one of the many industries innovating with AI and deep learning technologies: healthcare is one of the leading applications of AI.

Incorporating Sustainable Design in Medical Device Development

As the majority of hospitals incorporate sustainability into their purchasing decisions and countries regulate sustainable design (e.g. Brazil), it’s prudent for medical device manufacturers to consider sustainable design in their medical device development.

The Low Powered Internet of Things

Launched in June 2012, Internet Protocol version 6 (IPv6) is a network protocol that is often referred to as the next generation internet. Using IPv6 allows every device to have its own IP address to connect directly to the Internet.

Considerations for Wearable Device Development

Healthcare is among the fastest-growing segments of the $13 billion wearables market, due to the overwhelming need to monitor diseases and aging populations.

The Key Steps to Identify A Regulatory Requirements Strategy

When developing medical devices it is important to understand the regulatory landscape that is applicable to your particular device and to jump start the approval process with the appropriate regulatory agency/agencies.

The Design Requirements and Agency Expectations for Connected Devices

The design of wireless medical devices needs to include aspects of system design which are not always obvious. The FDA document Guidance for Industry and Food and Drug Administration Staff Document issued on August 14, 2013, is an excellent starting point for identifying design aspects of a wireless system that must operate and ‘co-exist’ with other diverse devices as well as multiple instances of itself.

Understanding The Value That Low Power Wide Area Network Technology Can Bring To Your Medical Or Consumer Device

With predictions for IoT-enabled devices to reach over 40 billion by 2020, it becomes critical to better understand the choices of connectivity solutions available currently.

The FDA Agile Practices In Medical Device Development Under IEC 62304

Agile methods are state-of-the-art for software developers and they can be adapted to IEC62304 in the highly regulated medical device field. The Association for the Advancement of Medical Instrumentation (AAMI) has issued a Technical Information Report, TIR45 Guidance on the use of AGILE practices in the development of medical device software

The FDA Applies Recommendations To Mobile Medical Applications

The use of Smart Phones to deliver and medical services to patients and their caregivers is becoming more and more ubiquitous.

The FDA, Cybersecurity and Coexistence for Bluetooth and Wi-Fi Enabled Devices

Integrating wireless technology into medical devices has numerous benefits that positively impact patient outcomes both by allowing caregivers real time access to patient data and by providing the ability to remotely program these devices.

Quicker Proof of Concept and Prototyping

Commercial product development using low cost computing platforms like the Raspberry Pi, the Arduino and the Odroid is on the rise.

Current Design Includes An Explosion of Blue Tooth LE (BLE) Applications

There has been an explosion of awesome BLE applications for games, sporting goods, medical devices, sensors, wire replacement and more. BLE transmits less data over shorter distances using much less power than Bluetooth.

Increasing Efficiency in Developing a Higher Quality Product

There are many advantages to using a Software Framework, the most important being the re-use of code that has been tested, thereby reducing programming and testing labor and time to market.

Enhancing Your Risk Management Process

Medical device companies are required to implement risk management processes in compliance with ISO 14971.