Join us as we explore groundbreaking innovations and discuss the critical role of regulatory compliance in advancing healthcare through cutting-edge technology.
Так как сам живу с валютного рынка, могу утвердительно сказать, что если кто то не ради игры
Navigate FDA regulations for medical device development. Gain insights into compliance, approval processes, and key considerations for market entry and regulatory adherence.
Discover marketing’s pivotal role in the medical device industry, driving awareness, adoption, and market success for innovative healthcare tech. Gain insights into tailored strategies.
Become part of a community of over 10,000 medical device professionals who are driving healthcare forward through innovation.
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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.
There is one crucial team member in the development process who can help ensure ultimate project success: the Systems Engineer.
The healthcare sector is undergoing a profound transformation with the advent of the Medical Internet of Things (Medical IoT) within the rapidly expanding realm of the Internet of Things (IoT).
This article emphasizes the vital role of human factors validation and usability testing in medical device development, ensuring safety, effectiveness, and user satisfaction.
Plan for an effective design transfer process to successfully transfer your product into a viable manufactured good that can pass quality assurance tests.
Exploring advancements in drug delivery combination devices, this article highlights their revolutionary impact on medical treatments, offering insights into improved efficacy, patient compliance, and therapeutic outcomes, paving the way for transformative healthcare solutions.
FDA Approval: Medical Device Regulations for Innovation and Patient Safety Navigating the extensive terrain of medical device
In the laboratory setting, the advent of AI has been nothing short of revolutionary. Instruments equipped with
CE marking is a certification that indicates conformity with health, safety, and environmental protection standards for products sold within the EEA.
A great idea combined with great design skills are not good enough to guarantee your product’s. See why the design process starts with end-users in mind.
Product development starts with idea generation – You can find some important phases of the new Product Development Process. Call us to know more!
It is important to emphasize that UX design goes beyond software and apps – it also applies to physical products and services or systems.
Darren is an accomplished, dynamic leader who founded Nectar, X-Naut, and BreathDirect. He is committed to improving the world through the synthesis of technology, science, and art. Under Darren’s leadership, Nectar is leveraging the latest advances in cutting-edge technology to transform medical device development and design. As part of his
Dr. Steve Wells holds a critical role in steering Nectar’s operations and defining its strategic direction. His impactful leadership has established a clear course for the company’s success. He has revitalized the company with a passion for maximizing impact through expert resource utilization since taking the helm in 2020. Steve has boosted Nectar’s portfolio, streamlined processes, and reinvigorated its innovation agenda, all with the goal of developing life-saving and impactful products. His background in senior leadership roles at Georg Fischer and his people-focused, results-driven leadership style make him an invaluable asset to our team. Steve’s extensive knowledge in chemistry, biocompatibility, and biology only adds to his value as a team member.
Adam Marten has worked in the aerospace and consumer products industries since 2006 with lead engineering experience in conceptual design, product development, analysis and performance qualification testing. Adam has experience leading a range of technical projects, including multiple structural analyses for military and aerospace applications. He has also worked directly with engineering teams to develop medical devices and laboratory instrumentation.
With over two decades of experience in healthcare innovation, Kerry has been instrumental in transforming patient care and improving patient outcomes across the globe. Her extensive knowledge and expertise in the cardiovascular and cardiothoracic operating room, as well as her experience in emergency medicine, geriatrics, pediatric psychiatry, and main OR, make her a versatile and valuable member of the team. From small hospitals to large teaching institutions, Kerry’s 20 years of experience with patient documentation, including the use of EPIC, Cerner, and Meditech electronic charting systems, have positioned her as a leader in her field. Her recent involvement in helping transition the Providence St. Vincent Medical Center’s Cardiac Surgery program from paper charting to electronic documentation further underscores her commitment to advancing the healthcare industry.
