Cutting Through The Noise With Nectar’s EMI Mitigation Services
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.
Nectar is ISO 13485:2016 certified – but what exactly does that mean?
The International Organization for Standardization (ISO) have established standards for quality and risk management of materials and processes. Learn more.
Ensure Your Medical Device Development Process Run Smoothly
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: What is it, and why is it important for medical device development?
User interface (UI) and user experience (UX) are two terms you will hear interchangeably with medical devices, but they actually mean different things.
Regulatory Expectations in Medical Device Development 101
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.
Why Systems Engineering is Critical In the Design & Manufacturing of Medical Devices
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.
Redefining Healthcare With IoT
Find advice from Nectar Product Development’s Director of Operations, Shannon McElfresh-Hall, about what the company looks for in Engineering graduates. Read more.
The Importance of Human Factors Validation and Usability Testing
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!
Planning to Succeed: Managing the Design Transfer Process
Plan for an effective design transfer process to successfully transfer your product into a viable manufactured good that can pass quality assurance tests.
Episode 5: Navigating the Complex Terrain of Medical Device Development: Challenges and Insights
In this engaging podcast episode, we delve into the intricate world of medical device development, shedding light…