3M - Designing a medical device?

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MedTech Intelligence

Volume 10 Issue No. 20

Business Analysis Combination Products Market Access Operations Product Development Quality/Regulatory
Featured Articles

Vyaire MedicalProduct Design Error Triggers Vyaire Medical Class I Recall

By MedTech Intelligence Staff

In the United States, the company has recalled nearly 360,000 AirLife Resuscitation Device and Broselow Convenience Kits due to a malfunction risk.

CybersecuritySecurity for Connected Devices

By John Turner, Starfish Medical

Why does anyone want to hack a medical device or steal medical data? The risk may appear low, but unfortunately this is not the case.

FDAFDA Publishes FDARA Mandated Report on Servicing of Medical Devices

By MedTech Intelligence Staff

The report discusses the quality, safety and effectiveness of medical device servicing by OEMs and third parties.


Devine Guidance

Christopher Devine, Ph.D., Devine Guidance International Inspection Equipment not Qualified Equates to Problems with FDA!

By Dr. Christopher Joseph Devine,
Devine Guidance International

All equipment must be qualified and calibrated for its intended use.


Stephanie Domas, MedSecSnowflake Syndrome Creates Cybersecurity Roadblocks

By Stephanie Domas, MedSec

There are too many unique needs on the part of both manufacturers and providers. More collaboration is needed.


More Articles »

Upcoming Events & Webinars

Sept. 2018September 13-14, 2018 - MedTech Product Claims - What Can You Say?
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Nov. 2018November 27-28, 2018 - Global Strategies for Combination Products Conference
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Nov. 2018November 29-30, 2018 - Advanced CAPA and Root Cause Analysis Workshop for Medical Device Companies
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Q1 2019Q1 2019 - Digital Health Technologies Conference
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Q1 2019Q1 2019 - Medical Cybersecurity - Remediation of Legacy Medical Devices
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Q1 2019Q1 2019 - MedTech Innovation Mergers & Acquisitions Workshop
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