-->
Google

ENVI Sends IVD Regulation to Plenary; Industry Balks at Three-Year Transition

Written on:October 2, 2013
Comments are closed

In vitro diagnostic devicemakers say they will need at least five years to collect and submit additional supportive clinical data on their products, two more than proposed in regulations adopted by the EU Parliament’s health committee Sept. 25.

Source: International Medical Device Regulatory Monitor

    

Sorry, the comment form is closed at this time.