IPX Rating Chart in Medical Device Design and Development
Commitment to IPX Ratings in Medical Device Innovation: Nectar’s Focus on Safety and Reliability In the realm
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Join us as we explore groundbreaking innovations and discuss the critical role of regulatory compliance in advancing healthcare through cutting-edge technology.
Commitment to IPX Ratings in Medical Device Innovation: Nectar’s Focus on Safety and Reliability In the realm
Decoding FDA Regulations: A Comprehensive Guide for Medical Device Developers Welcome to our blog series on medical
This blog explores the crucial intersection of compliance and safety within medical device labeling, emphasizing the importance of regulatory adherence to ensure patient well-being and legal compliance.
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This article delves into user interface design’s significance in medical device development, highlighting its crucial role in ensuring usability, safety, and user satisfaction, offering valuable insights for engineers and designers aiming to create effective and user-friendly medical devices.
There is one crucial team member in the development process who can help ensure ultimate project success: the Systems Engineer.
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.
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.
Nectar Product Development has redesigned a limp lengthening device that was released into the market for patients with limb length discrepancy (LLD).
The Medical Device and Diagnostic Industry (MD+DI) featured Nectar in an article to help guide companies ready to engage in product development.
Find some important human factors like Safety, Bias, Effective Design, and Product Assessment that help to create the best product designs. Read to know more.
BreathDirect’s BDR-19™ Critical Care Ventilator from California’s Nectar Product Development, Receives FDA Emergency Use Authorization
Nectar hosts Junior year students for an on-site workshop, and this year we kept up our tradition by hosting them virtually via Zoom. Read to know more.
Incorporate a user-interface design strategy ensures that all of your products meet all user needs and fulfill the intentional purposes required by the FDA.
Product Development firm develops emergency ventilator in 8 weeks during pandemic using an ISO 13485 QMS and user-center design.
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.