OM DENNE PODKAST 🔗

Opdateringsfrekvens:
bimonthly
Gjennomsnittlig lydlængde:
44 minutes
Gæsteinterviews
Engelsk
USA
8 episoder
siden 8. februar 2023
serial

Ældste episoder 🔗

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 N…

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SISTE EPISODER

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…
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 obje…
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 de…
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 regula…
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, p…
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 Palad…
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…
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Ansvarsfraskrivelse: Podkasten og kunstværket, det finnes indlejret på denne siden, er fra Nectar, som tilhører dens eier og ikke er tilknyttet eller godkjent av Listen Notes, Inc.