When it comes to designing and building novel medical devices to meet the needs of patients and healthcare systems, developers should rely on the core skills of engineering and design to inform their process. But there are “lessons learned” that are unique to the medical device development process. The team at Goddard has contributed to […]
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Human factors engineering: 3 practical tips for user-centered design
by Orlando Soto (Engineering Manager), Omar Bermudez (Senior Industrial Designer), and Sarah Faulkner (Director of Marketing) Human factors engineering is a critical – and in some industries, mandated – part of the product development process. The data generated from human factors activities can help you to create products that are useful and can stand up […]
Delivering quality – The ISO 13485 Certification
By Charlie Sears, Quality Manager, Goddard Inc. The medical device industry is one of the most highly regulated verticals worldwide. Devices and quality systems must satisfy stringent requirements before they can be marketed and sold in the U.S. and worldwide. The ISO 13485 standard specifies requirements for a quality management system (QMS) for an organization […]
