Medical Devices includes a session from a regulatory expert on how companies can align their research between regions.

January 13, 2026 - PRESSADVANTAGE - In the highly regulated field of medical device labeling translation, ensuring that ...

This week in Pedersen's POV, our senior editor argues against FDA's huge shift in digital health — made without public ...

Düsseldorf District Court issues preliminary injunction against Beijing Hanbaihan Medical Devices Co., Ltd. regarding ...

In a pair of guidance documents released Tuesday, the regulator clarified the types of wellness features and clinical ...

Etienne Nichols, a medical device guru and community manager at Greenlight Guru, recently posed an interesting question to his LinkedIn network: If you were in charge, what regulation would you change ...

In the United States, medical device regulation and intellectual property (IP) protection are governed by complex statutory and regulatory frameworks that are distinct from—but closely related to, and ...

The US Food and Drug Administration (FDA) is moving to relax regulatory requirements for low risk health and wellness ...

A recent study led by researchers at the Yale School of Medicine and Harvard Medical School found that a loophole in existing regulation has allowed manufacturers to acquire U.S. Food and Drug ...

In recent years, there has been an uptick in interest in the Chinese market from licensors based predominantly in the U.S., Canada, Europe, and South Korea. Factors encouraging the in-licensing of ...

GENEVA--(BUSINESS WIRE)--Medimaps Group, a Swiss/Global med-tech company specializing in image-processing software with AI capabilities for assessing bone health, announced today it received the ...

Great Britain is entering a new era of MedTech regulation, with major pre-market changes expected that are designed to ...