New materials regulations in the European Union mean medical devices have one more layer of red tape to cut through before they can reach the market.
Medical device makers looking to bring new products to the European market will find a new layer of regulation before they can attain CE Mark approval.
The European Commission's new hazardous substances restrictions now apply to medical devices for the 1st time, requiring that all products coming to the E.U. market after July 22, 2014, meet materials standards before they get market approval.
from MassDevice - FDA and Medical device business news and jobs for the medical device industry http://ift.tt/1ttQeGA
Cap comentari:
Publica un comentari a l'entrada