Team Member Spotlight: Mike Olichney, Lead Engineer December 6, 2022 Boulder iQ’s new lead engineer is a man of principles. “I’m a first principles guy,” says Mike of his approach to engineering. Referring to the reasoned thinking that requires breaking down a problem into its fundamentals, he operates on the basis that things should work […]
Manufacturing Strategies for Start-ups: Start Flexible. By Jim Kasic, Founder & Chairman, Boulder iQ December 5, 2022 Your medical device may have the potential to be groundbreaking, life-saving and marketable. But it won’t be any of those things unless you can manufacture it in a way that gets it to the market as quickly as […]
Melinda Sogo, Directory of Quality October 20, 2022 Think of quality management as a logic problem. That’s the key to Melinda Sogo’s approach. Much of quality management is about taking apart a regulation and figuring out how to meet its requirements in the most cost-effective way, she says. “It’s a logic problem: finding the intersection […]
4 Tips to Reduce EO Emissions Today Boulder iQ looks at the EO issue from the product side in light of recently released EPA report September 21, 2022 The U.S. Environmental Protection Agency (EPA) recently published a list of ethylene oxide (EO) sterilization plants around the country that may be linked to increased cases of […]
Medical Device Packaging Labels 101 Originally published on Med Device Online, March 16, 2022 Product labels that appear on device packages, admittedly, are not the most exciting part of medical device product design and development. They lack the excitement of scientific discovery, the cachet of human factors design, and even the rigor of testing. They’re often thought about […]
The Lure of the FDA Q-Sub Meeting: When (and When Not) to Call for One Part 1: Timing considerations Jim Kasic, Founder & Chairman, Boulder iQ Ah. The Q-Sub. The FDA loves Q-Sub meetings, manufacturers love to get FDA input and they’re free. What’s the issue? There is no issue – when product developers use […]
Unpacking Contracts: Fixed-Bid or Time and Materials We have many clients who come in asking if we do fixed-bid or time and materials (T&M) for our proposals. Now the simple “consulting” answer is that it depends. Fixed bid and T&M have a time and place where they work best. Fixed-bid contracts are exactly like they […]
Animal Study Mishaps: How to Prevent Mistakes Introduction Animal studies are an important aspect of any medical device product development program. Animal studies provide data and evidence needed for development and regulatory submission. It can illustrate the performance and efficacy of the device in a live biological system. The study can also provide evidence on […]
How to survive an FDA inspection! Part 2 Surviving an FDA Inspection Part 2 In Part 1 we discussed the key logistics involved with the FDA visiting your facility and the types of inspections they might wish to perform. Initial inspections, routine inspections and Quality System Surveillance Inspections are the most common. The FDA publishes […]
How to survive an FDA inspection! Part 1 It’s a Friday, late morning or early afternoon. You’re in the conference room with a few other executives of your medical device company. Also in the room is an inspector from the US Food and Drug Administration, the FDA. The inspector showed up the previous Monday for […]
