(no subject)
Law on clinical trials is not better than anal tags. No.
Prizes for anyone who can read this footnote without their eyes crossing. Note: every single directive has an official English title, for which I needed to find the equivalent on Google. Ew. And there are 30 pages of text plus zillions of these footnotes in font 8...
*weeps*
Directive 93/42/EEC of the European Commission of 14 June 1993 relating to medical devices (Legal gazette - J.O. no. L 169 of 12.7.1993, p. 1) modified by Directive 98/79/EC of the European Parliament and European Commission of 27 Oct. 1998 relating to medical devices and in-vitro diagnostics (J.O. no. L 331 of 7.12.1998, p.1) and by Directive 2000/70/EC of the European Parliament and European Commission of 16 Nov. 2000, modifying Directive 93/42/EEC by the Commission concerning medical devices incorporating stable derivates of blood or of human plasma (J.O. no. L 313 of 13.12.2000, p.22). The texts of the Directives quoted in this Ordinance can be obtained from the Swiss Information Centre for Technical Standards, Bürglistr. 29, 8400 Winterthur, or can be downloaded from: http://europa.eu.int/eur-lex/fr/index.html.
Directive 90/385/EEC of the European Commission of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices (J.O. no. L 189 of 20.7.1990, p. 17), modified by Directive 93/42/EEC of the European Commission of 14 June 1993 relating to medical devices and by Directive 93/68/EEC of the European Commission of 22 July 1993, modifying various EEC Directives (J.O. no. L 220 of 30.8.1993, p.1).
Had enough yet?
Prizes for anyone who can read this footnote without their eyes crossing. Note: every single directive has an official English title, for which I needed to find the equivalent on Google. Ew. And there are 30 pages of text plus zillions of these footnotes in font 8...
*weeps*
Directive 93/42/EEC of the European Commission of 14 June 1993 relating to medical devices (Legal gazette - J.O. no. L 169 of 12.7.1993, p. 1) modified by Directive 98/79/EC of the European Parliament and European Commission of 27 Oct. 1998 relating to medical devices and in-vitro diagnostics (J.O. no. L 331 of 7.12.1998, p.1) and by Directive 2000/70/EC of the European Parliament and European Commission of 16 Nov. 2000, modifying Directive 93/42/EEC by the Commission concerning medical devices incorporating stable derivates of blood or of human plasma (J.O. no. L 313 of 13.12.2000, p.22). The texts of the Directives quoted in this Ordinance can be obtained from the Swiss Information Centre for Technical Standards, Bürglistr. 29, 8400 Winterthur, or can be downloaded from: http://europa.eu.int/eur-lex/fr/index.html.
Directive 90/385/EEC of the European Commission of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices (J.O. no. L 189 of 20.7.1990, p. 17), modified by Directive 93/42/EEC of the European Commission of 14 June 1993 relating to medical devices and by Directive 93/68/EEC of the European Commission of 22 July 1993, modifying various EEC Directives (J.O. no. L 220 of 30.8.1993, p.1).
Had enough yet?