Medical Device Network on MSN
FDA announces regulatory exemptions for ‘non-medical grade’ devices
The US Food and Drug Administration (FDA) is moving to relax regulatory requirements for low risk health and wellness ...
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 ...
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 ...
These technologies are improving all the time. If they’re not making claims that they are medical grade, let’s let the market ...
The Elena and Miles Zaremski Law Medicine Forum presents: Medical Device Regulation: Going from Bad to Worse...or Better? with George Horvath Innovations in medical device technology hold the ...
FDA’s decision to limit regulations of non-medical grade wearables marks a notable shift toward regulatory restraint in digital health. FDA announced its plan to stop subjecting non-medical grade ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results