Saturday, December 7, 2019

Saturday, December 7, 2019

Latest News

FDA could be prohibiting terminal patients from life-saving treatments and medication

The world of pharmaceuticals and biotechnology is ever-growing and changing, but seemingly only behind closed doors.

FDA assesses duoenoscope contamination risk

The Food and Drug Administration oversees manufacturers’ postmark surveillance studies on new and significant health concerns in order to understand a device’s risks and to update policies on such risks.

Medical device makers likely to benefit from ‘similar product’ expedited approval process in 2019

Keeping pace with technology that seems to develop at the speed of light and getting medical treatments to the people who most need them as quickly as possible while still maintaining top standards and keeping patients safe is tricky for the U.S. Food and Drug Administration, but that is its job.

FDA Reporter