Delay for Swiss medtech law
This article was originally published in Clinica
Executive Summary
The revised Swiss medical devices law, which will transpose the EU's In Vitro Diagnostics Directive, is now expected in January 1 2002, six months later than orginally planned (see Clinica No 935, p 4). The new regulatory authority to oversee medicinal and therapeutic products, including medical devices, is also scheduled to be set up then.