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Nectar is an award-winning product development company based in southern California. Our product design and development process is an interdisciplinary approach combining industrial design, user experience design, mechanical engineering, and electrical engineering that ensures product designs are successfully executed into production. We’ve been helping clients design products that connect to their users and expand their markets for over 30 years. We are firm believers in the team approach to product developments, which is why we'd like to share our wisdom with like-minded individuals, hence why we've created this podcast. Join us as we take a deep-dive into common product development topics and share our views.
8 Episodes
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Join Nectar's CEO, Darren Saravis, and Industrial Design Manager, James Wilkin, as they delve into the world of User Centered Design. In this episode, Darren and James will discuss what User Centered Design is and how it's used within medical device development. They'll explain how Nectar integrates this approach into their process and the benefits that it brings to their clients. Whether you're a seasoned medical device developer or simply curious about the subject, this episode is a must-li...
In this episode, we will be discussing the best practices for conducting user research in medical device development. User research is an imperative step in the product development process, and it helps to ensure that medical devices are safe, effective, and meet the needs of the people who use them. Our speakers will discuss various aspects of user research, including how to recruit and screen participants, how to conduct interviews or surveys, and how to use different research method...
In this episode, we will be discussing the essence of industrial design and its role in shaping the world around us. From the initial spark of inspiration to the final product launch, we explore the multifaceted world of industrial design, showcasing how designers transform ideas into tangible objects that enrich our lives. We uncover the meticulous techniques and methodologies employed to strike the delicate balance between aesthetics and usability, leaving no stone unturned in the pursuit o...
In this episode, we explore the often overlooked role of industrial design in shaping medical devices. Medical devices are vital in healthcare, saving lives and enhancing patient care, yet industrial design's significance is often underestimated. We delve into the crucial role of industrial design, examining the unique challenges and opportunities it presents in medical device design. From cleanability and material properties to security, usability, risk mitigation, and human factors, we unco...
In the fast-evolving landscape of medical device development, ensuring safety, efficacy, and regulatory compliance is paramount. Join us in this episode as we dive into the intricate world of FDA clearance and ISO certification in the realm of medical devices. From understanding the rigorous regulatory processes to highlighting the importance of meeting these standards, we explore the challenges, benefits, and implications for both manufacturers and end-users. Learn how navigating through the...
Join host Sarah Clark and a panel of experts in this episode as they uncover the vital steps in medical device product development. With guest Mike Sleva, a seasoned professional in medical device marketing, you'll explore essential aspects of commercialization, the significance of branding, positioning, and the power of thorough market research. Whether you're a startup or a seasoned player, gain insights to stay competitive in this ever-evolving industry. Tune in for actionable strategies a...
In this episode, "FDA Regulations Guide for Medical Device Developers," listeners are taken on a comprehensive journey into the intricate world of FDA regulations governing medical device development. Through insightful discussions with industry experts, including Elaine Duncan from Paladin Medical, the podcast explores key concepts such as defining medical devices, understanding indications for use, and classifying devices according to FDA guidelines. The episode delves into the importance o...
In this episode of the MedTech Innovation 360, we delve into risk assessment and management within medical device development. Exploring the definitions of risk, we differentiate between risk assessment and risk management, stressing the importance of early identification and mitigation. Key points include the relationship between risk and hazards, the role of Failure Modes Effects Analysis (FMEA) in identifying potential failures, the significance of ISO 14971 as a guiding standard, and the ...
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