Danish Medicines Agency now responsible for GLP inspections of device trials
This article was originally published in RAJ Devices
Executive Summary
The Danish Medicines Agency has taken over responsibility for inspecting good laboratory practice trials of medical devices, an activity that previously fell within the remit of the Danish Accreditation and Metrology Fund, DANAK1.
You may also be interested in...
Global medtech alliance approves six new member associations
An emerging alliance of medical technology industry associations representing innovative companies that currently develop and manufacture 85% of the world's medical devices, diagnostics and equipment has approved the membership applications of six more associations, bringing the total number of members to 19.
Global medtech alliance approves six new member associations
An emerging alliance of medical technology industry associations representing innovative companies that currently develop and manufacture 85% of the world's medical devices, diagnostics and equipment has approved the membership applications of six more associations, bringing the total number of members to 19.
US FDA scrutiny of DTC genetic tests continues
The US FDA's devices unit has written to three genetic testing companies warning them that they may be marketing their products and services without clearance by the agency.