Shorten Your Medical Device Development Timeline Using These 3 Design Research Strategies

Design research can shorten the development process by making your FDA submission quicker and easier. Plus, you are making it more robust by doing the work now as opposed to later. Too many people wait until later in the process for this work and end up guessing on things or adding “filler” to their required usability data, which oftentimes the FDA can easily sniff out and flag. But by then it takes more time and money.

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Designing Your Device So it Gets Reimbursed

With this complete medical device engineering and design offering, IPS/Kablooe services ensure speed to market for medical devices, successful user adoption and assurance of market advantage.

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IPS Joins Kablooe to Launch New Partnership

With this complete medical device engineering and design offering, IPS/Kablooe services ensure speed to market for medical devices, successful user adoption and assurance of market advantage.

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How To Make A Better User Interface For Your Medical Device

Those of us who are in the design industry typically spend a lot of our time thinking about the person who is going to use our fabulous invention, and what the situation is like when they will be using it...

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Risk Mitigation For Homecare Devices

Mitigating risk is one of the cornerstone activities of medical device design. The FDA’s goal is to only approve devices that are safe and effective, which means all risk would necessarily be removed from the use of the device. However, the definition of “safe” can be debated among developers because all risk can never be fully removed from any device.

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Events

Oct 14

Kablooe Open House

October 14 @ 3:00 pm - 7:00 pm
Oct 18

SOLIDWORKS What’s New 2023

October 18 @ 3:00 pm - 7:00 pm
Nov 01

AM Medical Summit 2022

November 1 - November 3
Nov 02

Advanced Manufacturing Minneapolis

November 2 - November 3