How major medtech companies are responding to the looming EU MDR

Medtech companies that sell products in the European Union have a major deadline looming — one that’s already been put off once…….

Building a Better Supply Chain Through Unique Device Identification

Class I medical device companies have work to do, despite the UDI enforcement delay…….

EU MDR Approval: Performing the Literature Search

Under the new regulation, medtech manufacturers can no longer defend their claims with limited clinical data; the depth, breadth and scrutiny on clinical data is much more rigorous…….

How Is Medtech Impacted by a Strained US-China Relationship? A CEO Speaks Out

While some believe cutting ties with China would serve as an impetus for more goods to be made in America, some medtech leaders think it could be disastrous — especially during a pandemic…….

Medtech AI & Software Regulation in China: 5 Things to Know

Regulation in China of AI and software in life sciences is still developing in response to rapid tech advances. Will a shift in regulatory focus in China from point-in-time registration to whole-of-life scrutiny impact AI device approval?……

A Few New Challenges with EU MDR

Experts speaking at MD&M West offered strategies for preparing for the European Union's Medical Device Regulation.

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Preparing for the EU Medical Device Regulation

Despite a delay to the EU MDR, there are many changes for medical device manufacturers to put in motion now. Can freelance scientists help?

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Artificial Intelligence and Machine Learning-Based Medical Devices: A Products Liability Perspective

How will products liability law be applied to AI?

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3D Printing of PPE and Other Medical Devices

Consider the trade-offs of using 3D printing to address current supply demands of personal protective equipment.

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Proposal to Postpone EU Medical Device Regulation Underway

A delay of one year could allow authorities and industry to focus instead on urgent responses needed to address the COVID-19 pandemic.

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