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MEDFlix

June 17, 2015

3M Medical Materials and Technologies – Today’s Answers, Tomorrow’s Breakthroughs

A new generation of wearable medical devices, miniaturized “lab-on-a-chip” diagnostic tests and other life-enhancing innovations are being made possible, in part, through the use of technologies provided by the newly-relaunched 3M Medical Materials and Technologies group (formerly 3M Medical Specialties).

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June 9, 2015

The Miniaturization Power of Micro Molding

One of the key enabling technologies in the miniaturization trend is micro injection molding. The constant shrinking of devices has put a lot of pressure on designers and manufacturing services to produce more complex, tighter tolerances, and smaller components.

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June 5, 2015

Hot Topics in Risk Management & Medical Devices

By MedTech Intelligence Staff

Roberta Goode, president & CEO of Goode Compliance International, weighs in on the latest challenges medical device manufacturers are facing in risk management at the MedTech Intelligence HHE, Risk Assessment, & Recalls Conference in Washington, DC.

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Columns

March 29, 2017

Practical Advice for Your Regulatory Strategy

By MedTech Intelligence Staff
Susan Alpert, SFA Consulting, Global Regulatory Strategy

For companies in global markets, consider these three factors.

March 6, 2017

Should I Pursue Emerging Medtech Markets?

By MedTech Intelligence Staff
Matthew Hein, U.S. Department of Commerce

Many companies go for product approval in smaller markets first. Is that the right decision?

April 21, 2016

Connecting User Needs with Actionable Product Design Inputs

By MedTech Intelligence Staff

Identifying user needs and actually turning them into actionable inputs during the design process can be a challenge.

April 11, 2016

FDA Says Consider Device Context, Not Just Intended Use

By MedTech Intelligence Staff
FDA, Al Taylor, Risk

Device companies need to think about how their product interacts with systems and users.

March 4, 2016

MedTech Blunders in Risk Management

By MedTech Intelligence Staff
Jon Speer, risk management

A look at some common mistakes medical device companies make when approaching risk.

March 1, 2016

Consistency Needed in Addressing IEC 60601-1 3rd Edition Risk Management

By MedTech Intelligence Staff
Mark Leimbeck, UL

There’s a greater emphasis on being able to demonstrate competence in performing required activities.

February 12, 2016

Testing Devices Critical Part of Improving Patient Safety

By Maria Fontanazza
ECRI Instiute

This video demonstrates how ECRI Institute tests medical devices.

February 11, 2016

Why Duodenoscopes Are So Tough to Clean

By Maria Fontanazza
ECRI, duodenoscopes, endoscopes

Complexity of design and frequency of use play a large role in how effectively scopes are reprocessed.

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