Medical Device Design Guide — The Complete Development Process
Regardless of what type of medical device you develop, the FDA requires you to follow a regulated process. Each step of medical […]
Regardless of what type of medical device you develop, the FDA requires you to follow a regulated process. Each step of medical […]
Table of Contents After settling on a winning concept, prototype development is the next step in product development. In this phase, you will […]
Concept development is the part of the product development process where you will generate, evaluate, and refine your abstract ideas, turning them […]
DFM stands for Design for Manufacturing or Design for Manufacturability and is also sometimes referred to as DFMA, where the A represents […]
Human factors engineering is a complex and multi-disciplinary area of risk management. It involves knowledge integration from various scientific fields, including psychology […]
The challenge The medical device market is historically fueled by innovation. The robotic surgical space is an area with a lot of […]
3D printing is a prototyping method that “prints” a three-dimensional physical object in layers from a digital file. Compared to traditional prototyping […]
FMEA stands for Failure Mode and Effects Analysis and is a risk management tool for identifying potential failures. FMEA assesses the severity […]
Tyler Luneski is the latest addition to Synectic’s team of talented design and development engineers. Join us, as we sit down with […]
Biocompatibility testing is the best way to evaluate medical device safety. Through biocompatibility testing, the FDA confirms that either there are none […]
A practical guide to reducing qualification, compliance, manufacturing, and integration risk before production.
Learn how defense programs reduce risk related to qualification, compliance, environmental testing, manufacturability, and production scale-up.
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