New York Times calls for tightened medical device regulation from FDA

By Medisi America on 18 junio, 2019

The New York Times last Friday released an editorial calling for improved regulation on medical devices from the FDA, citing a number of recent controversial devices that have made headlines for injuries and deaths related to their use.

If you want to read more about this news click here.

www.massdevice.com/new-york-times-calls-for-tightened-medical-device-regulation-from-fda/

Posted in News.

← NewerUsing EEG data to diagnose Parkinson’s disease

Older →More than 1 million Class I medical device units recalled in Q1

Deja una respuesta Cancelar la respuesta

18 junio, 2019

5 Pediatric Orthopedic Devices you need to know

The National Capital Consortium for Pediatric Device Innovation recently recognized five pediatric orthopedic devices that could improve scoliosis treatment, clubfoot assessment, and surgical imaging. If you want to read more about this news click here.
30 diciembre, 2019

Researchers produce first laser ultrasound images of humans.

«Engineers have come up with an alternative to conventional ultrasound that doesn’t require contact with the body to see inside a patient. The new laser ultrasound technique leverages an eye- and skin-safe laser system to remotely image the inside of a person.» Read more
30 diciembre, 2019

Finding a non-invasive way to predict effectiveness of cancer therapy.

«Researchers have taken a critical step toward developing a non-invasive nuclear medicine technique that can predict the effectiveness of therapy for cancerous tumors, allowing for personalized, precision treatment.» Read more.
10 octubre, 2019

Study: Abbott, Edwards may have mislabeled hundreds of patient deaths

Abbott (NYSE:ABT) and Edwards Lifesciences (NYSE:EW) may have mislabeled patient deaths as injuries or device malfunctions in hundreds of FDA adverse event reports involving their transcatheter aortic or mitral valve replacement devices, according to a new study. The study by JAMA Internal Medicine editor Dr. Rita Redberg, former FDA unique device identification (UDI) external program manager Madris Tomes and others examined a total …

Deja una respuesta Cancelar la respuesta

Related Posts

5 Pediatric Orthopedic Devices you need to know

Researchers produce first laser ultrasound images of humans.

Finding a non-invasive way to predict effectiveness of cancer therapy.

Study: Abbott, Edwards may have mislabeled hundreds of patient deaths