Electromagnetic Interference (EMI) is the interference caused when an electronic device is exposed to an electromagnetic field. Any device that has electronic circuitry can be susceptible to EMI, and with the increase of more complex electronic devices, EMI has become more and more of an issue.
The International Organization for Standardization (ISO) have established standards for quality and risk management of materials and processes. Learn more.
Before you even reach the FDA approval stage, there are a few things you should keep in mind as you run through the medical device development process.
User interface (UI) and user experience (UX) are two terms you will hear interchangeably with medical devices, but they actually mean different things.
Having an idea for a medical device that can change the world is great, but is only the beginning. Make sure you understand the regulatory requirements.
Clinical development of a product or device is a tough. With such a difficult process, it’s no wonder why a Systems Engineering so valuable. Here’s why.
Find advice from Nectar Product Development’s Director of Operations, Shannon McElfresh-Hall, about what the company looks for in Engineering graduates. Read more.
Know about Human Factors Validation and Usability Testing and what is the Importance of this method in Medtech Product Development? Visit Nectar to learn more!
Plan for an effective design transfer process to successfully transfer your product into a viable manufactured good that can pass quality assurance tests.
In this engaging podcast episode, we delve into the intricate world of medical device development, shedding light…