Recall Readiness: Combating Recall Fatigue

By Maria Fontanazza, Editor-in-Chief

At next week’s Medical Device Recall conference, FDA and industry experts will discuss best practices and procedures.

Commodity Malware:
What Medical Device Manufacturers Should Know

By Stephanie Domas, Battelle

Just because your device isn’t specifically targeted by hackers doesn’t mean it isn’t vulnerable to cybersecurity threats.

Breathalyzer Helps Patients Non-Invasively Check Blood Glucose

By MedTech Intelligence Staff

The finger-prick alternative may help diabetic patients more effectively monitor their condition.

Eye Care Needs Rising
Quickly in Asia

By Ames Gross, Pacific Bridge Medical

A lack of quality, locally made products opens the door for Western device companies.

Featured Quote

To incorporate sustainability into a product development organization, some training is required, because people often don’t understand how to incorporate sustainability into the design of a medical device.

— Ann Meitz, 3M

Devine Guidance

‘No’ Means No

By Christopher Devine, Ph.D.,
Devine Guidance International

Why would a company intentionally ignore FDA and market a device that hasn’t been cleared by the agency?

Dirty Endoscopes:
FDA Outlines Risks of Cross Contamination for Device Components

By MedTech Intelligence Staff

The agency released a guidance document with product design recommendations to help prevent contamination from device components.