Brussels, 28/06/2002 (Agence Europe) - The European Commission has decided to send a reasoned opinion to France, which has not yet completed transposition of the 1998 Directive on in vitro diagnostic medical devices. The Directive establishes technical specifications guaranteeing a high level of quality and safety for a very broad range of products (reagents, control materials, apparatus, instruments, software, etc.) intended for in vitro examination of specimens from the human body. It was...